Restricted immunoglobulin heavy chain mice

ABSTRACT

Mice having a restricted immunoglobulin heavy chain locus are provided, wherein the locus is characterized by a single polymorphic human V H  gene segment, a plurality of human D H  gene segments and a plurality of J H  gene segments. Methods for making antibody sequences that bind an antigen (e.g., a viral antigen) are provided, comprising immunizing a mouse with an antigen of interest, wherein the mouse comprises a single human V H  gene segment, a plurality of human D H  gene segments and a plurality of J H  gene segments, at the endogenous immunoglobulin heavy chain locus.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit under 35 USC § 119(e) of U.S. Provisional Application Ser. No. 61/658,459, filed Jun. 12, 2012, U.S. Provisional Application Ser. No. 61/597,969, filed Feb. 13, 2012 and U.S. Provisional Application Ser. No. 61/547,974, filed Oct. 17, 2011, which applications are hereby incorporated by reference in their entirety.

FIELD

Non-human animals that are genetically engineered at an immunoglobulin heavy chain variable (V) region locus (or in a transgene) to make antibodies from a restricted number of immunoglobulin heavy chain variable (V_(H)) segments (or a single V_(H) segment) and/or variants thereof. Non-human animals that have a human heavy chain variable domain derived from a single immunoglobulin heavy chain variable gene segment, e.g., human immunoglobulin V_(H)1-69 gene segment or human V_(H)1-2 gene segment. Methods for making antibody sequences in non-human animals that are useful for binding pathogens, including human pathogens.

BACKGROUND

Non-human animals, e.g., mice, have been genetically engineered to be useful tools in methods for making antibody sequences for use in antibody-based human therapeutics. Mice with humanized variable region loci (e.g., V_(H), D_(H), and J_(H) genes, and V_(L) and J_(L) genes) are used to generate cognate heavy and light chain variable domains for use in antibody therapeutics. Other mice are available that generate fully human antibodies with cognate heavy and light chains.

Human antibody therapeutics are engineered based on desired characteristics with respect to certain pre-selected antigens. Humanized mice are immunized with the pre-selected antigens, and the immunized mice are used to generate antibody populations from which to identify high-affinity cognate heavy and light variable domains with desired binding characteristics. Some humanized mice, such as those having a humanization of just variable regions at endogenous mouse loci, generate populations of B cells that are similar in character and number to wild-type mouse B cell populations. As a result, an extremely large and diverse population of B cells is available in these mice from which to screen antibodies, reflecting a large number of different immunoglobulin rearrangements, to identify heavy and light variable domains with the most desirable characteristics.

But not all antigens provoke an immune response that exhibits a very large number of rearrangements from a wide selection of variable (V) segments. That is, the human humoral immune response to certain antigens is apparently restricted. The restriction is reflected in clonal selection of B cells that express only certain V segments that bind that particular antigen with sufficiently high affinity and specificity. Some such antigens are clinically significant, i.e., a number are well-known human pathogens. A presumption arises that the V segment expressed in the human immune response is a V segment that, in combination with a human D and a human J segment, is more likely to generate a useful high affinity antibody than a randomly selected V segment that has not been observed in a human antibody response to that antigen.

It is hypothesized that natural selection, over millennia, has selected the most efficient foundation or base from which to design a most effective weapon for neutralizing human pathogens—a clonally selected V segment. There is a need in the art for more and superior antibodies that bind and/or neutralize antigens such as the pathogens discussed above. There is a need to more rapidly generate useful sequences from selected V segments, including polymorphic and/or somatically mutated selected V segments and to more rapidly generate useful populations of B cells having rearrangements of the V segments with various D and J segments, including somatically mutated versions thereof, and in particular rearrangements with unique and useful CDR3s. There is a need for biological systems, e.g., non-human animals (such as, e.g., mice, rats, rabbits, etc.) that can generate therapeutically useful antibody variable region sequences from pre-selected V segments in increased number and diversity than, e.g., can be achieved in existing modified animals. There is a need for biological systems engineered to have a committed humoral immune system for clonally selecting antibody variable sequences derived from restricted, pre-selected V segments, including but not limited to cognate human heavy and light chain variable domains, useful in the manufacture of human antibody-based therapeutics against selected antigens, including certain human pathogens.

There is a need in the art for therapeutic antibodies that are capable of neutralizing viral antigens, e.g., HIV and HCV, including antigen-specific antibodies containing heavy chains derived from a single human variable segment, and for a system that produces a diverse source of antibodies from which to select therapeutic antibody sequences. There is also a need for further methods and non-human animals for making useful antibodies, including antibodies that comprise a repertoire of heavy chains derived from a single human V_(H) segment and having a diverse set of CDR sequences, and including such heavy chains that express with cognate human light chain variable domains. Methods are needed for selecting CDRs for immunoglobulin-based binding proteins that provide an enhanced diversity of binding proteins from which to choose, and enhanced diversity of immunoglobulin variable domains, including compositions and methods for generating somatically mutated and clonally selected immunoglobulin variable domains for use, e.g., in making human therapeutics.

SUMMARY

Genetically modified immunoglobulin loci are provided that comprise a restricted number of different heavy chain variable region gene segments (i.e., V genes, V_(H) genes, V_(H) gene segments, or V gene segments), e.g., no more than one, two, or three different V genes; or no more than one V gene segment family member present, e.g., in a single copy or in multiple copies and/or comprising one or more polymorphisms.

Loci are provided that are capable of rearranging and forming a gene encoding a heavy chain variable domain that is derived from a V_(H) gene repertoire that is restricted, e.g., that is a single V_(H) gene segment or selected from a plurality of polymorphic variants of the single V_(H) gene segment. Modified immunoglobulin loci include loci that comprise human immunoglobulin sequences are provided, e.g., a human V segment operably linked to a human or (or human/non-human chimeric) non-human immunoglobulin constant sequence (and in operable linkage with, e.g., a D and/or a J segment). Modified loci that comprise multiple copies of a single V_(H) gene segment, including wherein one or more of the copies comprises a polymorphic variant, are provided. Modified loci that comprise multiple copies of a single V_(H) segment, operably linked with one or more D segments and one or more J segments, operably linked to a non-human immunoglobulin constant sequence, e.g., a mouse or rat sequence, are provided. Non-human animals comprising such humanized loci are also provided.

Non-human animals are provided that have a reduced immunoglobulin heavy chain variable gene segment complexity (i.e., a limited number of heavy chain variable gene segments, or a limited heavy chain variable gene repertoire), wherein the reduced immunoglobulin heavy chain variable gene segment complexity is characterized by the presence of no more than one or no more than two heavy chain variable gene segments, and wherein the heavy chain variable genes present are operably linked to a human or non-human constant region sequence.

Non-human animals are provided that have a reduced immunoglobulin heavy chain variable gene segment complexity (e.g., a single V_(H) gene segment, or a limited number of V_(H) gene segments that are polymorphic variants of a single V_(H) gene segment), wherein the reduced immunoglobulin heavy chain variable gene segment complexity is characterized by the presence of a single V_(H) gene segment or a plurality of V_(H) gene segments that are polymorphic forms of a single V_(H) gene segment (e.g., V_(H) gene segments associated with high copy number and/or polymorphism in humans), and wherein the heavy chain variable genes present are operably linked to a human or non-human constant region sequence. In various embodiments, the heavy chain variable genes present are operably linked to one or more D and/or one or more J gene segments in the germline of the non-human animal.

Non-human animals are provided that comprise an immunoglobulin heavy chain variable locus (e.g., on a transgene or as an insertion or replacement at an endogenous non-human animal heavy chain variable locus) that comprises a single V_(H) segment operably linked to a D and/or J gene segment. In various embodiments, the single V_(H) gene segment is operably linked to one or more D and/or one or more J gene segments at the endogenous immunoglobulin heavy chain variable gene locus of the non-human animal.

Non-human animals are provided that are modified at their immunoglobulin heavy chain variable region loci to delete all or substantially all (e.g., all functional segments, or nearly all functional segments) endogenous immunoglobulin V_(H) segments and that comprise a human V_(H)1-69 segment (or a human V_(H)1-2 segment) operably linked to a D and J segment or a J segment at the endogenous immunoglobulin heavy chain variable region locus of the non-human animal.

Non-human animals are also provided that are modified at their immunoglobulin heavy chain variable region loci to render the endogenous variable region loci incapable of rearranging to form a functional heavy chain comprising endogenous variable region gene segments; wherein the non-human animals comprise a single human variable gene segment (a human V_(H)1-2 or a human V_(H)1-69 gene segment) operably linked to a D and a J segment or a J segment at the endogenous immunoglobulin heavy chain variable region locus of the non-human animal.

Non-human animals are provided that comprise a restricted number (e.g., no more than one, or no more than two) of heavy chain gene segments operably linked to a human or non-human constant region sequence. In one embodiment, the no more than one or no more than two heavy chain gene segments linked to the constant region sequence are on a transgene, e.g., are at a position other than an endogenous heavy chain locus.

Methods are provided for making human immunoglobulin sequences in non-human animals. In various embodiments, the human immunoglobulin sequences are derived from a repertoire of immunoglobulin V sequences that consist essentially of a single human V segment, e.g., V_(H)1-69 or V_(H)1-2, and one or more D and J segments or one or more J segments. Methods for making human immunoglobulin sequences in non-human animals, tissues, and cells are provided, wherein the human immunoglobulin sequences bind a pathogen.

Methods are provided for making mice characterized by a restricted immunoglobulin heavy chain locus, wherein the restriction is with respect to the number of immunoglobulin V_(H) gene segments. In various aspects, the restriction is to one or no more than two, or a single V_(H) gene family member (e.g., one or more V_(H) alleles, variants, or polymorphic variants thereof). In various aspects, the heavy chain locus further comprises one or more D_(H) gene segments and one or more J_(H) gene segments. In various aspects, the V_(H), D_(H) and J_(H) gene segments are human. In various aspects, the V_(H), D_(H) and J_(H) gene segments are operably linked to a non-human constant region (e.g., an IgM and/or an IgG). In various aspects, the constant region is a mouse or rat constant region.

In one aspect, a method for making a mouse having a restricted immunoglobulin heavy chain locus is provided, comprising introducing a nucleic acid construct as described herein into a mouse embryonic stem (ES) cell, and isolating or identifying a mouse ES cell that comprises the nucleic acid construct.

In one embodiment, the nucleic acid construct comprises a single human V_(H) gene segment, one or more human D_(H) gene segments, and one or more human J_(H) gene segments. In one embodiment, the nucleic acid construct comprises one or more site-specific recombination sites (e.g., a IoxP or a Frt site).

In one aspect, a mouse made using a targeting vector, nucleic acid sequence, or cell as described herein is provided. In various embodiments, the targeting vector, nucleic acid sequence or cell comprises a DNA sequence that contains a single human V_(H) gene segment (or polymorphic variants thereof), one or more human D_(H) gene segments, and one or more human J_(H) gene segments operably linked to a non-human constant gene.

In one aspect, a method for making a mouse comprising a restricted immunoglobulin heavy chain locus is provided, comprising replacing a mouse immunoglobulin heavy chain locus with a human genomic sequence comprising a single human V_(H) gene segment (or polymorphic variants thereof), one or more human D_(H) gene segments, and one or more human JH gene segments, wherein the human V_(H), D_(H) and J_(H) gene segments are capable of rearranging to form a chimeric heavy chain that contains a human variable domain operably linked to a non-human constant region. In one embodiment, the non-human constant region is a mouse or rat constant region.

In various aspects, the non-human animals are rodents. In various aspects, the rodents are mice and/or rats.

In one aspect, a modified immunoglobulin heavy chain locus is provided that comprises a heavy chain V segment repertoire that is restricted with respect to the identity of the V segment, and that comprises one or more D segments and one or more J segments, or one or more J segments. In one embodiment, the heavy chain V segment is a human segment. In one embodiment, the one or more D segments are human D segments. In one embodiment, the one or more J segments are human J segments. In one embodiment, the one or more D segments and one or more J segments are human D and human J segments.

In one embodiment, the modified locus is a non-human locus. In one embodiment, the non-human locus is modified with at least one human immunoglobulin sequence.

In one embodiment, the restriction is to one V segment family member. In one embodiment, the one V segment family member is present in two or more copies. In one embodiment, the one V segment family member is present as two or more variants (e.g., two or more polymorphic forms of the V segment family member). In one embodiment, the one V segment is a human V segment family member. In one embodiment, the one V segment family member is present in a number of variants as is observed in the human population with respect to that variant. In one embodiment, the V segment family member is selected from Table 1. In one embodiment, the V segment family member is present in a number of variants as shown, for each V segment, in a number of alleles from 1 allele to the number of alleles shown in the right column of Table 1.

In one embodiment, the restriction is to a human V_(H)1-69 gene segment. In one embodiment, the human V_(H)1-69 gene segment is present in two or more copies. In one embodiment, the human V_(H)1-69 gene segment is present as two or more variants (e.g., two or more polymorphic forms the human V_(H)1-69 gene). In one embodiment, the human V_(H)1-69 gene segment is present in a number of variants as is observed in the human population with respect to the human V_(H)1-69 gene segment. In one embodiment, the human V_(H)1-69 gene segment is selected from Table 2. In one embodiment, the human V_(H)1-69 gene segment is present in a number of variants as shown, for each V_(H)1-69 gene segment, in a number of alleles from one allele to the number of alleles shown in Table 2.

In one embodiment, the restriction is to a human V_(H)1-2 gene segment. In one embodiment, the human V_(H)1-2 gene segment is present in two or more copies. In one embodiment, the human V_(H)1-2 gene segment is present as two or more variants (e.g., two or more polymorphic forms the human V_(H)1-2 gene). In one embodiment, the human V_(H)1-2 gene segment is present in a number of variants as is observed in the human population with respect to the human V_(H)1-2 gene segment. In one embodiment, the human V_(H)1-2 gene segment is selected from Table 3. In one embodiment, the human V_(H)1-2 gene segment is present in a number of variants as shown, for each V_(H)1-2 gene segment, in a number of alleles from one allele to the number of alleles shown in Table 3.

In one aspect, a heavy chain immunoglobulin locus is provided that comprises a single functional human V segment. In one embodiment, the single functional human V segment is selected from a V_(H)1-2, V_(H)1-3, V_(H)1-8, V_(H)1-18, V_(H)1-24, V_(H)1-45, V_(H)1-46, V_(H)1-58, V_(H)1-69, V_(H)2-5, V_(H)2-26, V_(H)2-70, V_(H)3-7, V_(H)3-9, V_(H)3-11, V_(H)3-13, V_(H)3-15, V_(H)3-16, V_(H)3-20, V_(H)3-21, V_(H)3-23, V_(H)3-30, V_(H)3-30-3, V_(H)3-30-5, V_(H)3-33, V_(H)3-35, V_(H)3-38, V_(H)3-43, V_(H)3-48, V_(H)3-49, V_(H)3-53, V_(H)3-64, V_(H)3-66, V_(H)3-72, V_(H)3-73, V_(H)3-74, V_(H)4-4, V_(H)4-28, V_(H)4-30-1, V_(H)4-30-2, V_(H)4-30-4, V_(H)4-31, V_(H)4-34, V_(H)4-39, V_(H)4-59, V_(H)4-61, V_(H)5-51, V_(H)6-1, V_(H)7-4-1, and a V_(H)7-81 segment.

In one embodiment, the single functional human V segment is a V_(H)1-69 segment; in a specific embodiment, the single functional human V segment is present in 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13 polymorphic forms found in the human population. In one embodiment, the single functional human V segment is a V_(H)1-2 segment; in a specific embodiment, the single functional human V segment is present in 1, 2, 3, 4, or 5 polymorphic forms found in the human population.

In one embodiment, the heavy chain immunoglobulin locus is a modified locus of a non-human animal. In one embodiment, the modified non-human immunoglobulin heavy chain locus is present in the non-human animal at a position in the genome in which the corresponding unmodified non-human locus is found in the wild-type non-human animal. In one embodiment, the modified non-human immunoglobulin heavy chain locus is present on a transgene in a non-human animal.

In one embodiment, the single functional human V gene segment is a V_(H)1-69 gene segment. In one embodiment, the V_(H)1-69 gene segment comprises SEQ ID NO: 34. In one embodiment, the V_(H)1-69 gene segment is derived from SEQ ID NO: 34. In one embodiment, the V_(H)1-69 gene segment is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical to SEQ ID NO: 34.

In one embodiment, the single functional human V gene segment is encoded by the nucleotide sequence of SEQ ID NO: 34.

In one embodiment, the single functional human V gene segment is a V_(H)1-2 gene segment. In one embodiment, the V_(H)1-2 gene segment comprises SEQ ID NO: 60. In one embodiment, the V_(H)1-2 gene segment is derived from SEQ ID NO: 60. In one embodiment, the V_(H)1-2 gene segment is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical to SEQ ID NO: 60.

In one embodiment, the single functional human V gene segment is encoded by the nucleotide sequence of SEQ ID NO: 60.

In one embodiment, the single functional human V segment is operably linked to one or more D segments and one or more J segments, or one or more J segments. In one embodiment, the V segment and one or more D and/or J segments are operably linked to an immunoglobulin heavy chain constant region sequence. In one embodiment the immunoglobulin heavy chain constant region sequence is selected from a C_(H)1, a hinge, a C_(H)2, a C_(H)3 sequence, and a combination thereof. In one embodiment, the C_(H)1, hinge, C_(H)2, C_(H)3, or combination thereof are each non-human endogenous constant sequences. In one embodiment, at least one of the C_(H)1, hinge, C_(H)2, C_(H)3, or combination thereof is a human sequence. In a specific embodiment, the C_(H)1 and/or hinge are human sequences.

In one aspect, a modified endogenous non-human immunoglobulin heavy chain locus is provided, comprising a replacement of all functional V gene segments with a single human V gene segment (or a single human V gene segment present in multiple polymorphic forms or copy number), wherein the non-human immunoglobulin heavy chain locus is incapable of rearrangement to form a heavy chain variable gene that is derived from a V gene segment other than the single human V gene segment (or one of the polymorphic forms or copies).

In one embodiment, the single human V gene segment is V_(H)1-69. In one embodiment, the single human V gene segment is V_(H)1-2.

In one embodiment, the locus comprises at least one human or non-human D_(H) gene segment, and one human or non-human J_(H) gene segment. In a specific embodiment, the locus comprises a human D_(H) gene segment and a human J_(H) gene segment. In a specific embodiment, the locus comprises a human J_(H) gene segment. In another specific embodiment, the locus comprises a human V_(H)1-69 gene segment (present as a single copy or multiple copies of different polymorphic variants), all functional human D_(H) gene segments, and all functional human J_(H) gene segments. In another specific embodiment, the locus comprises a human V_(H)1-2 gene segment (present as a single copy or multiple copies of different polymorphic forms), all functional human D_(H) gene segments, and all functional human J_(H) gene segments. In one embodiment, the human V, D, and J gene segments (or V and J gene segments) are operably linked to a mouse constant region gene at an endogenous mouse heavy chain locus. In a specific embodiment, the mouse heavy chain locus comprises a wild-type repertoire of mouse immunoglobulin constant region sequences.

In one aspect, a genetically modified non-human animal is provided, wherein the only functional immunoglobulin heavy chain V gene segment of the non-human animal is selected from a human V_(H)1-2, V_(H)1-3, V_(H)1-8, V_(H)1-18, V_(H)1-24, V_(H)1-45, V_(H)1-46, V_(H)1-58, V_(H)1-69, V_(H)2-5, V_(H)2-26, V_(H)2-70, V_(H)3-7, V_(H)3-9, V_(H)3-11, V_(H)3-13, V_(H)3-15, V_(H)3-16, V_(H)3-20, V_(H)3-21, V_(H)3-23, V_(H)3-30, V_(H)3-30-3, V_(H)3-30-5, V_(H)3-33, V_(H)3-35, V_(H)3-38, V_(H)3-43, V_(H)3-48, V_(H)3-49, V_(H)3-53, V_(H)3-64, V_(H)3-66, V_(H)3-72, V_(H)3-73, V_(H)3-74, V_(H)4-4, V_(H)4-28, V_(H)4-30-1, V_(H)4-30-2, V_(H)4-30-4, V_(H)4-31, V_(H)4-34, V_(H)4-39, V_(H)4-59, V_(H)4-61, V_(H)5-51, V_(H)6-1, V_(H)7-4-1, and V_(H)7-81 gene segment. In one embodiment, the heavy chain V gene segment is a human V_(H)1-69 gene segment. In one embodiment, the heavy chain V gene segment is a human V_(H)1-2 gene segment.

In one aspect, a genetically modified non-human animal is provided, wherein the non-human animal comprises a single functional human V_(H) gene segment (present as a single copy or multiple copies of different polymorphic forms), and wherein the non-human animal is substantially incapable of forming a rearranged immunoglobulin heavy chain variable domain gene that lacks the single functional human V_(H) gene segment (or one of the polymorphic forms or copies).

In one aspect, a genetically modified non-human animal is provided, wherein the only immunoglobulin heavy chain variable region expressed in the non-human animal is derived from one of a human segment selected from a human V_(H)1-2, V_(H)1-3, V_(H)1-8, V_(H)1-18, V_(H)1-24, V_(H)1-45, V_(H)1-46, V_(H)1-58, V_(H)1-69, V_(H)2-5, V_(H)2-26, V_(H)2-70, V_(H)3-7, V_(H)3- 9, V_(H)3-11, V_(H)3-13, V_(H)3-15, V_(H)3-16, V_(H)3-20, V_(H)3-21, V_(H)3-23, V_(H)3-30, V_(H)3-30-3, V_(H)3-30-5, V_(H)3-33, V_(H)3-35, V_(H)3-38, V_(H)3-43, V_(H)3-48, V_(H)3-49, V_(H)3-53, V_(H)3-64, V_(H)3-66, V_(H)3-72, V_(H)3-73, V_(H)3-74, V_(H)4-4, V_(H)4-28, V_(H)4-30-1, V_(H)4-30-2, V_(H)4-30-4, V_(H)4-31, V_(H)4-34, V_(H)4-39, V_(H)4-59, V_(H)4-61, V_(H)5-51, V_(H)6-1, V_(H)7-4-1, and V_(H)7-81 gene segment. In one embodiment, the human segment is a V_(H)1-69 segment. In one embodiment, the human segment is a V_(H)1-2 segment. In one embodiment, the only immunoglobulin heavy chain variable region expressed by the mouse is derived from a single V segment family member, and in one embodiment the only immunoglobulin heavy chain variable region is derived from a polymorphic variant of the single V segment family member.

In one aspect, a non-human animal comprising a restricted immunoglobulin heavy chain V gene segment repertoire is provided, wherein the non-human animal further comprises one or more human immunoglobulin κ light chain variable segments (V_(κ)). In one embodiment, the one or more V_(κ) segments are operably linked to one or more human J segments. In a specific embodiment, the J segments are human J_(κ) segments. In another specific embodiment, the non-human animal does not express an immunoglobulin λ light chain. In another specific embodiment, the non-human animal does not comprise a functional human or functional endogenous immunoglobulin λ light chain variable locus.

In one embodiment, the non-human animal is a rodent. In one embodiment, the rodent is a mouse.

In one embodiment, the non-human animal comprises a replacement at the endogenous non-human immunoglobulin V_(κ) locus of all or substantially all functional endogenous V_(κ) segments with one or more functional human V_(κ) segments. In a further specific embodiment, the replacement is with all or substantially all functional human immunoglobulin V_(κ) segments.

In one embodiment, the non-human animal comprises a replacement at the endogenous non-human immunoglobulin V_(κ) locus of all or substantially all functional endogenous V_(κ) gene segments with human V_(κ) gene segments selected from V_(κ)4-1, V_(κ)5-2, V_(κ)7-3, V_(κ)2-4, V_(κ)1-5, V_(κ)1-6, V_(κ)3-7, V_(κ)1-8, V_(κ)1-9, V_(κ)2-10, V_(κ)3-11, V_(κ)1-12, V_(κ)1-13, V_(κ)2-14, V_(κ)3-15, V_(κ)1-16, V_(κ)1-17, V_(κ)2-18, V_(κ)2-19, V_(κ)3-20, V_(κ)6-21, V_(κ)1-22, V_(κ)1-23, V_(κ)2-24, V_(κ)3-25, V_(κ)2-26, V_(κ)1-27, V_(κ)2-28, V_(κ)2-29, V_(κ)2-30, V_(κ)3-31, V_(κ)1-32, V_(κ)1-33, V_(κ)3-34, V_(κ)1-35, V_(κ)2-36, V_(κ)1-37, V_(κ)2-38, V_(κ)1-39, V_(κ)2-40, and a combination thereof.

In one embodiment, the non-human animal comprises a replacement at the endogenous non-human immunoglobulin J_(κ) locus of all or substantially all functional endogenous non-human immunoglobulin J_(κ) segments with one or more functional human immunoglobulin J_(κ) segments. In a further specific embodiment, the replacement is with all or substantially all functional human immunoglobulin J_(κ) segments.

In one embodiment, the non-human animal comprises a replacement at the endogenous non-human immunoglobulin J_(κ) locus of all or substantially all functional endogenous non-human immunoglobulin J_(κ) gene segments with human J_(κ) gene segments selected from J_(κ)1, J_(κ)2, J_(κ)3, J_(κ)4, J_(κ)5, and a combination thereof.

In a specific embodiment, the non-human animal comprises an immunoglobulin heavy chain variable region locus that comprises a repertoire of V segments consisting essentially of a single V segment and/or polymorphic variants thereof. In one embodiment, the single immunoglobulin heavy chain V segment is a human V_(H)1-69 segment, and the non-human animal further comprises a replacement of all functional non-human D_(H) segments with all functional human D_(H) segments, and further comprises a replacement of all functional non-human J_(H) segments with all functional human J_(H) segments, and wherein the immunoglobulin heavy chain variable region locus is operably linked to a human or non-human constant region gene sequence. In a specific embodiment, the constant region gene sequence is an endogenous non-human constant region gene sequence. In a specific embodiment, the non-human animal rearranges segments at the non-human immunoglobulin heavy chain locus to form a gene encoding heavy chain variable region comprising a human V_(H)1-69 sequence, a human D_(H) sequence, a human J_(H) sequence, and a mouse constant region sequence.

In a specific embodiment, the non-human animal comprises an immunoglobulin heavy chain variable region locus that comprises a repertoire of V segments consisting essentially of a single V segment and/or polymorphic variants thereof. In one embodiment, the single immunoglobulin heavy chain V segment is a human V_(H)1-2 segment, and the non-human animal further comprises a replacement of all functional non-human D_(H) segments with all functional human D_(H) segments, and further comprises a replacement of all functional non-human J_(H) segments with all functional human J_(H) segments, and wherein the immunoglobulin heavy chain variable region locus is operably linked to a human or non-human constant region gene sequence. In a specific embodiment, the constant region gene sequence is an endogenous non-human constant region gene sequence. In a specific embodiment, the non-human animal rearranges segments at the non-human immunoglobulin heavy chain locus to form a gene encoding heavy chain variable region comprising a human V_(H)1-2 sequence, a human D_(H) sequence, a human J_(H) sequence, and a mouse constant region sequence.

In one embodiment, a B cell is provided that comprises the rearranged gene. In a specific embodiment, the B cell is from a mouse as described that has been immunized with an antigen of interest, and the B cell encodes an antibody that specifically binds the antigen of interest. In one embodiment, the antigen of interest is a pathogen. In a specific embodiment, the pathogen is selected from an influenza virus, a hepatitis virus (e.g., hepatitis B or hepatitis C virus), and a human immunodeficiency virus. In a specific embodiment, the B cell encodes a somatically mutated, high affinity (e.g., about 10⁻⁹ K_(D) or lower) antibody comprising a human light chain variable region (e.g., a human K light chain variable region) that specifically binds the antigen of interest.

In one aspect, a non-human animal comprising a restricted immunoglobulin heavy chain V segment repertoire is provided, wherein the non-human animal comprises one or more human λ light chain variable (V_(λ)) segments. In one embodiment, the one or more human V_(λ) segments are operably linked to one or more human J segments. In a specific embodiment, the J segments are human J_(λ) segments. In another specific embodiment, the non-human animal does not express a κ light chain. In another specific embodiment, the non-human animal does not comprise a functional human or non-human κ light chain variable locus.

In one embodiment, the non-human animal comprises a replacement of all or substantially all functional non-human immunoglobulin V_(λ) segments with one or more functional human immunoglobulin V_(λ) segments. In a further specific embodiment, the replacement is with all or substantially all functional human immunoglobulin V_(λ) segments.

In one embodiment, the non-human animal comprises a replacement of all or substantially all functional non-human V_(λ) segments with a fragment of cluster A of the human λ light chain locus. In a specific embodiment, the fragment of cluster A of the human λ light chain locus comprises human V_(λ) gene segments V_(λ)3-27 through V_(λ)3-1.

In one embodiment, the non-human animal comprises a replacement of all or substantially all functional non-human V_(λ) segments with a fragment of cluster B of the human λ light chain locus. In a specific embodiment, the fragment of cluster B of the human λ light chain locus comprises human V_(λ) gene segments V_(λ)5-52 through V_(λ)1-40.

In one embodiment, the non-human animal comprises a replacement of all or substantially all functional non-human V_(λ) segments with a fragment of cluster A and a fragment of cluster B of the human λ light chain locus, wherein as a result of the replacement comprise human V_(λ) gene segments V_(λ)5-52 through V_(λ)3-1.

In one embodiment, the non-human animal comprises a replacement of all or substantially all functional non-human V_(λ) segments with at least 12 human V_(λ) gene segments, at least 28 human V_(λ) gene segments, or at least 40 human V_(λ) gene segments.

In one embodiment, the non-human animal comprises a replacement of all or substantially all functional non-human immunoglobulin J_(λ) gene segments with one or more functional human immunoglobulin J_(λ) gene segments. In a further specific embodiment, the replacement is with all or substantially all functional human immunoglobulin J_(λ) gene segments. In various embodiments, the functional human J_(λ) gene segments include J_(λ)1, J_(λ)2, J_(λ)3 and J_(λ)7.

In a specific embodiment, the non-human animal comprises an immunoglobulin heavy chain variable (V_(H)) region locus that comprises only a single V_(H) segment, wherein the single V_(H) segment is a human V_(H)1-69 segment or a human V_(H)1-2 segment, and further comprises a replacement of all functional non-human D_(H) segments with all functional human D_(H) segments, and further comprises a replacement of all functional non-human J_(H) segments with all functional human J_(H) segments, and wherein the V_(H) region locus is operably linked to a human or non-human constant region gene sequence. In a specific embodiment, the constant region gene sequence is a non-human constant region gene sequence, e.g., an endogenous non-human constant gene sequence. In a specific embodiment, the non-human animal rearranges segments at the non-human immunoglobulin heavy chain locus to form a gene encoding an immunoglobulin heavy chain variable region comprising a human V_(H)1-69 sequence (or a human V_(H)1-2 sequence), a human D_(H) sequence, a human J_(H) sequence, and an endogenous non-human constant region sequence.

In one embodiment, a B cell is provided that comprises the rearranged gene. In a specific embodiment, the B cell is from a non-human animal as described that has been immunized with an antigen of interest, and the B cell encodes an antibody that specifically binds the antigen of interest. In one embodiment, the antigen is a human protein selected from a ligand, a cell surface receptor and an intracellular protein. In one embodiment, the antigen of interest is a pathogen. In a specific embodiment, the pathogen is selected from an influenza virus, a hepatitis virus (e.g., hepatitis B or hepatitis C virus), and a human immunodeficiency virus. In a specific embodiment, the B cell encodes a somatically mutated, high affinity (e.g., about 10^(<9) K_(D) or lower) antibody comprising a human light chain variable region (e.g., a human λ light chain variable region) that specifically binds the antigen of interest.

In one aspect, a non-human animal comprising a restricted immunoglobulin V_(H) segment repertoire is provided, wherein the non-human animal comprises a human V_(H)1-69 segment (or a human V_(H)1-2 segment) on a transgene, wherein the human V_(H)1-69 segment is operably linked on the transgene to a human or non-human D_(H) segment, and/or a human or non-human J segment, and the transgene further comprises a human or non-human constant region gene, or a chimeric human/non-human constant region (e.g., a C_(H)1, hinge, C_(H)2, C_(H)3 or combination thereof wherein at least one sequence is non-human, e.g., selected from hinge, C_(H)2, and C_(H)3 and/or hinge). In one embodiment, the non-human animal is a mouse or rat and the non-human D, J, and/or constant region gene is a mouse or rat gene or chimeric human/mouse or rat.

In one embodiment, the non-human animal comprises a transgene that comprises an immunoglobulin light chain variable region locus that comprises one or more human immunoglobulin V_(λ) gene segments and J_(λ) gene segments, or one or more human immunoglobulin V_(κ) gene segments and J_(κ) gene segments, and a human immunoglobulin κ or λ light chain constant region gene, such that the transgene rearranges in the non-human animal to form a rearranged immunoglobulin κ or λ light chain gene. In various embodiments, the human V_(κ) and J_(κ) gene segments are those described herein. In various embodiments, the human V_(λ) and J_(λ) gene segments are those described herein.

In a specific embodiment, the non-human animal comprises a transgene having an immunoglobulin heavy chain variable locus that comprises a single V segment that is a human V_(H)1-69 segment (or a human V_(H)1-2 segment), one or more human D segments, one or more human J segments, and a human constant gene operably linked to the heavy chain variable locus, such that the mouse expresses from the transgene a fully human antibody derived from the V_(H)1-69 segment (or the V_(H)1-2 segment). In one embodiment, the non-human animal does not comprise a functional endogenous immunoglobulin heavy chain variable region locus. In a specific embodiment, the non-human animal comprises a nonfunctional endogenous immunoglobulin heavy chain variable region locus that comprises a deletion of an endogenous non-human D_(H) and/or endogenous non-human J_(H) segment, such that the non-human animal is incapable of rearranging the endogenous immunoglobulin heavy chain variable region locus to form a rearranged non-human antibody gene. In a specific embodiment, the non-human animal comprises a deletion of a switch sequence operably linked to an endogenous mouse heavy chain constant region. In a specific embodiment, the switch sequence is a non-human (e.g., mouse) μ switch sequence. In another embodiment, the non-human animal further comprises a lack of a functional endogenous light chain variable locus selected from an immunoglobulin κ locus and an immunoglobulin λ locus. In a specific embodiment, the non-human animal comprises a deletion of a J_(κ) and/or a J_(λ) sequence, such that the non-human animal is incapable of rearranging an endogenous non-human immunoglobulin κ light chain and/or an endogenous non-human immunoglobulin λ light chain variable region to form a rearranged endogenous non-human immunoglobulin κ light chain and/or a rearranged endogenous non-human immunoglobulin λ light chain gene.

In one embodiment, the non-human animal comprises a deletion of an endogenous non-human immunoglobulin κ light chain sequence that results in a functional knockout of the endogenous non-human immunoglobulin κ light chain. In one embodiment, the non-human animal comprises a deletion of an endogenous non-human immunoglobulin λ light chain sequence that results in a functional knockout of the endogenous non-human immunoglobulin λ light chain.

In one aspect, the non-human animal comprises a functionally silenced endogenous immunoglobulin heavy chain variable gene locus, and comprises a restricted repertoire of human heavy chain variable gene segments (e.g., no more than one, or no more than two). In one embodiment, the functional silencing comprises a modification of an endogenous non-human heavy chain variable gene locus selected from a deletion, an insertion, an inversion, and a combination thereof.

In one aspect, a rodent is provided that comprises an immunoglobulin V_(H) repertoire derived from no more than one human V_(H) segment or one or more polymorphs thereof, from a D segment selected from a repertoire of one or more D segments, and from a J segment derived from a repertoire of one or more J segments. In one embodiment, the rodent rearranges the human V_(H) segment, a human D segment, and a human J segment and forms a rearranged human heavy chain sequence that is operably linked to a human or a rodent constant region sequence. In one embodiment, the human and/or rodent constant region sequence is selected from a C_(H)1, a hinge, a C_(H)2, a C_(H)3, and a combination thereof. In one embodiment, the rodent expresses an immunoglobulin light chain that comprises a human variable domain, wherein the light chain is cognate with a human heavy chain domain derived from the rearranged human heavy chain sequence. In one embodiment, the rodent does not express a polypeptide sequence selected from a non-human heavy chain variable domain, a non-human light chain variable domain, and a combination thereof.

In one embodiment, the human V_(H) segment is present in 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, or 19 or more polymorphic variants, wherein each polymorphic variant is operably linked to a D and/or J segment such that each polymorphic variant is capable for rearranging and forming a rearranged heavy chain variable domain with any of the one or more D segments and any of the one or more J segments. In one embodiment, the rodent is a mouse or a rat. In one embodiment, the repertoire of D segments comprises two or more D segments. In one embodiment, the repertoire of J segments comprises two or more J segments. In one embodiment, the D and/or J segments are human segments.

In one aspect, a nucleic acid construct is provided that comprises a sequence encoding a single human immunoglobulin V_(H) segment and/or polymorphic variants thereof and one or more D_(H) and one or more J sequences, wherein the construct comprises at least one homology arm homologous to a non-human immunoglobulin heavy chain variable locus, or a recombinase recognition site (e.g., a lox site). In one embodiment, the V segment is a V_(H)1-69 segment or a V_(H)1-2 segment.

In one aspect, a nucleic acid construct is provided; comprising a nucleic acid sequence encoding a single human immunoglobulin heavy chain V segment, wherein the single V_(H) segment is a V_(H)1-69 (or V_(H)1-2) segment. In one embodiment, the construct comprises a site-specific recombinase recognition site. In one embodiment, the construct comprises a first mouse homology arm upstream of the V_(H)1-69 (or V_(H)1-2) segment and a second mouse homology arm downstream of the V_(H)1-69 (or V_(H)1-2) segment, and wherein the first mouse homology arm is homologous to a region of a mouse chromosome immediately upstream of a mouse immunoglobulin heavy chain variable region but not including a functional mouse immunoglobulin heavy chain variable segment. In one embodiment, the construct comprises SEQ ID NO: 3. In one embodiment, the construct comprises SEQ ID NO: 70.

In one aspect, the restricted single V_(H) segment is in a non-human animal, or the restricted V_(H) segment is at a non-human immunoglobulin heavy chain locus (e.g., in situ or in a transgene), and the non-human animal or non-human immunoglobulin heavy chain locus is selected from a mouse, rat, rabbit, pig, bovine (e.g., cow, bull, buffalo), deer, sheep, goat, chicken, cat, dog, ferret, primate (e.g., marmoset, rhesus monkey) locus or animal. In a specific embodiment, the non-human animal or locus is a mouse or a rat locus.

In one aspect, a cell or tissue is provided, wherein the cell or tissue is derived from a non-human animal as described herein, and comprises a restricted V_(H) segment repertoire. In one embodiment, the V_(H) segment repertoire is restricted to a single V_(H) segment family member and/or polymorphic variants thereof. In a specific embodiment, the single V_(H) segment is a human V_(H)1-69 segment or a human V_(H)1-2 segment. In one embodiment, the cell or tissue is derived from spleen, lymph node or bone marrow of the non-human animal.

In one embodiment, the cell is an ES cell. In one embodiment, the cell is a B cell. In one embodiment, the cell is a germ cell.

In one embodiment, the tissue is selected from connective, muscle, nervous and epithelial tissue. In a specific embodiment, the tissue is reproductive tissue.

In one embodiment, the cell and/or tissue derived from a mouse as described herein are isolated for use in one or more ex vivo assays. In various embodiments, the one or more ex vivo assays include measurements of physical, thermal, electrical, mechanical or optical properties, a surgical procedure, measurements of interactions of different tissue types, the development of imaging techniques, or a combination thereof.

In one embodiment, the non-human animal is a mouse.

In one aspect, a non-human embryo is provided comprising a restricted heavy chain V_(H) segments as described herein. In one embodiment, the embryo comprises an ES donor cell that comprises the restricted V_(H) segment, and host embryo cells.

In one embodiment, the non-human animal is a mouse.

In one aspect, a non-human cell comprising a chromosome or fragment thereof of a non-human animal as described herein. In one embodiment, the non-human cell comprises a nucleus of a non-human animal as described herein. In one embodiment, the non-human cell comprises the chromosome or fragment thereof as the result of a nuclear transfer.

In one aspect, a nucleus derived from a non-human animal as described herein is provided. In one embodiment, the nucleus is from a diploid cell that is not a B cell.

In one aspect, a pluripotent, induced pluripotent, or totipotent cell derived from a non-human animal as described herein is provided. In a specific embodiment, the cell is a mouse embryonic stem (ES) cell.

In one aspect, a non-human induced pluripotent cell comprising a restricted V_(H) segment repertoire is provided. In one embodiment, the induced pluripotent cell is derived from a non-human animal as described herein.

In one aspect, a hybridoma or quadroma is provided, derived from a cell of a non-human animal as described herein. In one embodiment, the non-human animal is a mouse or rat.

In one aspect, a lymphocyte of a non-human animal as described herein is provided. In one embodiment, the lymphocyte is a B cell.

In one aspect, mouse cells and mouse embryos are provided, including but not limited to ES cells, pluripotent cells, and induced pluripotent cells, that comprise genetic modifications as described herein. Cells that are XX and cells that are XY are provided. Cells that comprise a nucleus containing a modification as described herein are also provided, e.g., a modification introduced into a cell by pronuclear injection.

In one aspect, an antibody variable domain sequence made in a non-human animal as described herein is provided.

In one aspect, a human therapeutic is provided, comprising an antibody variable domain comprising a sequence derived from a non-human animal as described herein.

In one aspect, a method of obtaining an antibody variable region sequence from a non-human animal is provided, wherein the antibody variable region sequence is derived from a human V_(H)1-69 segment or a V_(H)1-2 segment, wherein the method comprises (a) immunizing a non-human animal with an antigen of interest, wherein the non-human animal comprises a replacement at the endogenous immunoglobulin heavy chain locus of all or substantially all non-human variable segments with a single human variable segment, wherein the single human variable segment is a V_(H)1-69 segment or a V_(H)1-2 segment, and wherein the non-human animal is substantially incapable of forming a immunoglobulin heavy chain variable region sequence that is not derived from a human V_(H)1-69 segment or a V_(H)1-2 segment; (b) allowing the non-human animal to mount an immune response with respect to the antigen of interest; and, (c) identifying or isolating an immunoglobulin heavy chain variable region sequence of the non-human animal, wherein the antibody binds the antigen of interest.

In one embodiment, the single human variable segment is a V_(H)1-69 segment.

In one embodiment, the antibody variable region sequence is derived from SEQ ID NO: 34. In one embodiment, the antibody variable region sequence is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical to SEQ ID NO: 34. In one embodiment, the antibody variable region sequence comprises SEQ ID NO: 34.

In one embodiment, the single human variable segment is a V_(H)1-2 segment.

In one embodiment, the antibody variable region sequence is derived from SEQ ID NO: 60. In one embodiment, the antibody variable region sequence is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical to SEQ ID NO: 60. In one embodiment, the antibody variable region sequence comprises SEQ ID NO: 60.

In one embodiment, the immune response to the antigen is characterized by an antibody titer that is about 6×10⁴ to about 5×10⁵ times greater than two times background as determined in an ELISA assay. In a specific embodiment, the antibody titer is about 1×10⁵ to about 2×10⁵ times greater than two times background as determined in an ELISA assay. In a specific embodiment, the antibody titer is about 1.5×10⁵ times greater than two times background as determined in an ELISA assay. In one embodiment, the antigen is a human cell surface receptor.

In one aspect, a method for generating a repertoire of human antibody variable regions in a non-human animal is provided, wherein the human heavy chain variable regions of the repertoire are derived from the same V_(H) gene family member and one of a plurality of D_(H) segments and one of a plurality of J_(H) segments, wherein the repertoire is characterized by having heavy chain immunoglobulin FR1 (framework 1), CDR1, FR2, CDR2, and FR3 sequences from a single V_(H) gene family member. In one embodiment, the repertoire is further characterized by having a plurality of different CDR3+FR4 sequences.

In one embodiment, the single V_(H) gene family is selected from V_(H) family 1, 2, 3, 4, 5, 6, and 7. In a specific embodiment, the single V_(H) gene family is V_(H) family 1. In one embodiment, the single V_(H) gene family member is selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, and V_(H)3-23. In a specific embodiment, the single V_(H) gene family member is V_(H)1-69. In a specific embodiment, the single V_(H) gene family member is V_(H)1-2.

In one embodiment, the repertoire comprises heavy chain FR1, CDR1, FR2, CDR2 and FR3 sequences derived from a V_(H)1-69 segment. In a specific embodiment, the repertoire comprises heavy chain FR1, CDR1, FR2, CDR2 and FR3 sequences derived from SEQ ID NO: 35. In a specific embodiment, the repertoire comprises heavy chain FR1, CDR1, FR2, CDR2 and FR3 sequences of SEQ ID NO: 35.

In one embodiment, the repertoire comprises heavy chain FR1, CDR1, FR2, CDR2 and FR3 sequences derived from a V_(H)1-2 segment. In a specific embodiment, the repertoire comprises heavy chain FR1, CDR1, FR2, CDR2 and FR3 sequences derived from SEQ ID NO: 61. In a specific embodiment, the repertoire comprises heavy chain FR1, CDR1, FR2, CDR2 and FR3 sequences of SEQ ID NO: 61.

In one aspect, a biological (i.e., in vivo) system is provided for generating a plurality of different human CDR3 sequences reflecting a plurality of rearrangements of a single human V_(H) gene segment with a plurality of human D and J segments, wherein the system generates human heavy chain variable domains characterized by having human FR1-CDR1-FR2-CDR2-FR3 sequences that are identical but for somatic hypermutations, wherein the heavy chain variable domains are characterized by being somatically hypermutated and derived from a single human V_(H) gene segment and a plurality of human D and J segments; wherein the system comprises a genetically modified non-human animal (e.g., a rodent, e.g., a mouse or rat) as described herein.

In one embodiment, the single human V_(H) gene segment is selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, and V_(H)3-23. In one embodiment, the single human V_(H) gene segment is V_(H)1-69. In one embodiment, the single human V_(H) gene segment is V_(H)1-2. In one embodiment, the single human V_(H) gene segment is identified in Table 1. In one embodiment, the single human V_(H) gene segment is identified in Table 2. In one embodiment, the single human V_(H) gene segment is identified in Table 3.

In one aspect, an in vivo method for generating a plurality of heavy chain CDR sequences derived from rearrangements of a single human V_(H) gene segment with a plurality of human D and J segments is provided, wherein the method generates human heavy chain variable domains characterized by having human FR1-CDR1-FR2-CDR2-FR3 sequences that are identical but for somatic hypermutations, wherein the heavy chain variable domains are characterized by being somatically hypermutated and derived from a single human V_(H) gene segment and a plurality of human D and J segments; wherein the system comprises a genetically modified non-human animal (e.g., a rodent, e.g., a mouse or rat) as described herein.

In one embodiment, the method comprises exposing a non-human animal as described herein to an antigen of interest, allowing the non-human animal to develop an immune response to the antigen, wherein the immune response generates the plurality of heavy chain CDR sequences derived from rearrangements of the single human V_(H) gene segment with one of the human D and one of the human J segments, and identifying a set of heavy chain CDRs that bind the antigen. In one embodiment, the method comprises isolating from the animal a nucleic acid sequence that encodes a human V_(H) domain that comprises the heavy chain CDRs.

In one embodiment, the heavy chain CDR sequences are derived from a rearrangement of a human V_(H)1-69 gene segment. In one embodiment, the heavy chain CDR sequences are derived from a rearrangement of a human V_(H)1-2 gene segment.

In one aspect, a method for generating a plurality of different CDR3 and FR4 sequences in a non-human animal is provided, comprising exposing a non-human animal that comprises an immunoglobulin heavy chain variable gene locus with a V_(H) segment repertoire restricted to a single V_(H) segment family member to an antigen of interest, allowing the non-human animal to develop an immune response to the antigen, wherein the immune response generates a B cell repertoire whose heavy chain variable domains are each derived from the single V_(H) segment family member and that comprise a plurality of different CDR3 and FR4 sequences.

In one embodiment, the singe V_(H) segment family member is human. In one embodiment, the non-human animal is selected from a mouse, a rat, and a rabbit. In one embodiment, the antigen of interest is selected from a ligand, a receptor, an intracellular protein and a secreted protein. In one embodiment, the antigen of interest is a human pathogen as described herein.

In one embodiment, the single human V_(H) gene family member is selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, and V_(H)3-23. In one embodiment, the single human V_(H) gene family member is V_(H)1-69. In one embodiment, the single human V_(H) gene family member is V_(H)1-2. In one embodiment, the single human V_(H) gene family member is identified in Table 1. In one embodiment, the single human V_(H) gene family member is identified in Table 2. In one embodiment, the single human V_(H) gene family member is identified in Table 3.

In one aspect, a nucleotide sequence encoding an immunoglobulin variable region made in a non-human animal as described herein is provided.

In one aspect, an immunoglobulin heavy chain or immunoglobulin light chain variable region amino acid sequence of an antibody made in a non-human animal as described herein is provided.

In one aspect, an immunoglobulin heavy chain or immunoglobulin light chain variable region nucleotide sequence encoding a variable region of an antibody made in a non-human as described herein is provided.

In one aspect, an antibody or antigen-binding fragment thereof (e.g., Fab, F(ab)₂, scFv) made in a non-human animal as described herein is provided.

In one aspect, a mouse having a restricted immunoglobulin heavy chain locus characterized by the presence of a single human V_(H) gene segment, one or more human D_(H) gene segments, and one or more human J_(H) gene segments is provided, wherein the single human V_(H) gene segment is at an endogenous mouse locus and the V_(H) gene segment is operably linked to the one or more human D_(H) gene segments, the one or more human J_(H) gene segments, and to an endogenous immunoglobulin heavy chain constant gene.

In one embodiment, the mouse further comprises a humanized immunoglobulin light chain locus comprising one or more human V_(L) gene segments, and one or more human J_(L) gene segments, wherein the human V_(L) gene segments and the human J_(L) gene segments are operably linked to a non-human immunoglobulin light chain constant region gene. In a specific embodiment, the human V_(L) and J_(L) gene segments are at an endogenous mouse light chain locus, and wherein the non-human immunoglobulin light chain constant region gene is a mouse gene.

In one embodiment, the humanized immunoglobulin light chain locus is on a transgene, and the constant region gene is selected from mouse, rat, and human.

In one embodiment, the human V_(L) and J_(L) gene segments are V_(κ) and J_(κ) gene segments. In one embodiment, the human V_(L) and J_(L) gene segments are V_(λ) and J_(λ) gene segments

In one aspect, a non-human animal is provided, wherein the non-human animal has a B cell repertoire that expresses immunoglobulin heavy chain variable domains derived from a single V segment family member. In one embodiment, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90, or at least 95% of the B cell repertoire of the non-human animal immunoglobulin heavy chain variable domain expressed in the B cell repertoire is derived from the same V segment family member. In a specific embodiment, the percentage is at least 90%. In one embodiment, the B cell repertoire consists essentially of peripheral (blood) B cells. In one embodiment, the B cell repertoire consists essentially of splenic B cells. In one embodiment, the B cell repertoire consists essentially of bone marrow B cells. In one embodiment, the B cell repertoire consists essentially of peripheral B cells, splenic B cells, and bone marrow B cells.

In one aspect, a genetically modified non-human animal is provided, wherein more than 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or more than 90% of the B cells of the non-human animal that express a heavy chain immunoglobulin variable domain express a heavy chain immunoglobulin variable domain derived from a single V_(H) gene segment family member. In one embodiment, at least 75% of the B cells of the non-human animal that express an immunoglobulin heavy chain variable domain express an immunoglobulin heavy chain variable domain derived from the single V_(H) gene segment family member. In a specific embodiment, the percentage is at least 90%. In one embodiment, all of the B cells that express a heavy chain domain that is derived from the single V_(H) gene family member.

In one aspect, a genetically modified mouse is provided that makes an antigen-specific B cell population in response to immunization with an antigen of interest, wherein at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or more than 90%, of said antigen-specific B cell population expresses immunoglobulin heavy chains that are all derived from the same V_(H) gene segment. In one embodiment, at least 75% of the antigen-specific B cell population expresses immunoglobulin heavy chains derived from the same V_(H) gene segment. In one embodiment, all of the antigen-specific B cells express a heavy chain that is derived from the same V_(H) gene segment.

In one aspect, a non-human animal comprising a restricted V_(H) gene segment repertoire is provided, wherein the restriction is to a human V_(H)1-69 gene segment or a V_(H)1-69 gene segment that is at least about 75.5%, 76.5%, 86.7%, 87.8%, 94.9%, 96.9%, 98%, or 99% identical to a V_(H)1-69*01 gene segment. In a specific embodiment, the restricted repertoire is selected from one or more of the V_(H)1-69 variants of FIG. 15.

In one aspect, a non-human animal comprising a restricted V_(H) gene segment repertoire is provided, wherein the restriction is to a human V_(H)1-2 gene segment or a V_(H)1-2 gene segment that is at least about 94.9%, 95.9%, 96.9%, 98%, or 99% identical to a V_(H)1-2 gene segment. In a specific embodiment, the restricted repertoire is selected from one or more of the V_(H)1-2 variants of FIG. 18.

In one embodiment, the non-human animal is a mouse.

In one embodiment, the mouse exhibits an immunophenotype having a characteristic of a higher ratio of mature B cells to immature B cells as compared to a wild type mouse. In a specific embodiment, the ratio is calculated from B cells harvested from spleen. In one embodiment, the mouse exhibits a population of mature B cells of about 1×10⁷. In one embodiment, the mouse exhibits a population of immature B cells of about 0.5×10⁷. In one embodiment, the mouse exhibits a ratio of mature B cells to immature B cells in the spleen of the mouse that is about 1.5-fold to about 2-fold higher than exhibited by a wild type mouse.

In one embodiment, the ratio is calculated from B cells harvested from bone marrow. In a specific embodiment, the mouse exhibits a population of mature B cells of about 3×10⁵. In one embodiment, the mouse exhibits a population of immature B cells of about 7×10⁵. In one embodiment, the mouse exhibits a ratio of mature B cells to immature B cells in the bone marrow of the mouse that is about 3-fold, or about 3.3-fold higher than exhibited by a wild type mouse.

In one embodiment, the mouse exhibits an immunophenotype having a characteristic of a higher number of pro B cells in the bone marrow as compared to a wild type mouse. In a specific embodiment, the mouse exhibits a population of pro B cells in the bone marrow of the mouse that is about 2.5-fold to about 3-fold higher than exhibited in the bone marrow of a wild type mouse. In a specific embodiment, the mouse exhibits a population of pro B cells in the bone marrow of the mouse that is about 2.75-fold higher than exhibited in the bone marrow of a wild type mouse.

In one embodiment, the mouse exhibits an immunophenotype having a characteristic selected from the group consisting of a CD19⁺ splenic B cell population that is about 80% of a wild-type B cell, a CD3⁺ splenic T cell population that is about the same as a wild type mouse, and a combination thereof.

In one embodiment, the mouse comprises a lymphocyte population whose % CD19⁺ B cells in spleen are about the same as a wild-type mouse. In one embodiment, the number of CD19⁺ B cells per spleen of the mouse is at least about 50% of the number of CD19⁺ B cells per spleen of a wild-type mouse.

In one embodiment, the non-human animal comprises at least about 75% to about 80% of CD19⁺ B cells in bone marrow as compared with a wild-type mouse.

In one embodiment, the total number of CD19⁺ bone cells per femur of the mouse is non less than about 30%, 40%, 50%, 60%, or 75% of the total number of CD19+ bone marrow cells in a wild-type mouse.

In one embodiment, the mouse expresses IgD and IgM at about the same level as observed in a wild-type mouse.

In one aspect, a mouse comprising a restricted human V_(H) segment repertoire is provided, further comprising a humanized immunoglobulin light chain variable segment locus, wherein the ratio of λ to κ light chains expressed in the mouse is about the same as in a wild-type mouse.

In one aspect, a mouse is provided, comprising a restricted immunoglobulin heavy chain locus characterized by the presence of a single V_(H) gene segment, one or more D_(H) gene segments, and one or more J_(H) gene segments, wherein the single V_(H) gene segment is a polymorphic V_(H) gene segment.

In one embodiment, the polymorphic V_(H) gene segment is a human V_(H) gene segment that is associated with a high copy number in human populations. In one embodiment, the human V_(H) gene segment is selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, V_(H)3-23, or a polymorphic variant thereof. In a specific embodiment, the human V_(H) gene segment is a V_(H)1-69 gene segment. In another specific embodiment, the human V_(H) gene segment is a V_(H)1-2 gene segment.

In one embodiment, the single V_(H) gene segment is operably linked to a human, mouse, or chimeric human/mouse immunoglobulin constant region gene. In a specific embodiment, the immunoglobulin constant region gene is a mouse constant region gene. In one embodiment, the immunoglobulin constant gene comprises a human sequence selected from a human C_(H)1, a human hinge, a human C_(H)2, a human C_(H)3, and a combination thereof. In one embodiment, the mouse constant gene is at an endogenous immunoglobulin heavy chain locus.

In one embodiment, the mouse further comprises a human immunoglobulin V_(L) gene segment operably linked to a J gene segment and a light chain constant gene. In a specific embodiment, the V_(L) gene segment and/or the J gene segment are selected from a human κ gene segment and a human λ gene segment. In one embodiment, the V_(L) and/or J gene segments are human κ gene segments.

In various embodiments, the mouse comprises a deletion of all or substantially all endogenous V_(H) gene segments.

In various embodiments, the non-human animal comprises an inactivated endogenous heavy chain variable gene locus. In various embodiments, the inactivated endogenous heavy chain variable gene locus is not operably linked to an endogenous heavy chain constant region gene.

In one aspect, a mouse is provided, wherein the mouse is characterized by the expression of serum immunoglobulin, wherein greater than 80% of the serum immunoglobulin comprises a human heavy chain variable domain and a cognate human light chain variable domain, wherein the human heavy chain variable domain is derived from a V_(H) gene segment repertoire consisting essentially of a single human V_(H) gene segment and/or polymorphic variants thereof.

In one embodiment, the single human V_(H) gene segment is a human V_(H)1-69 gene segment and/or polymorphic variants thereof. In one embodiment, the single human V_(H) gene segment is a human V_(H)1-2 gene segment and/or polymorphic variants thereof.

In one aspect, a mouse is provided, comprising, in its germline, a replacement at an endogenous immunoglobulin heavy chain locus of all or substantially all endogenous V_(H) gene segments with a single human V_(H) gene segment and/or polymorphic variants thereof. In one embodiment, the single human V_(H) gene segment is a human V_(H)1-69 gene segment and/or polymorphic variants thereof. In one embodiment, the single human V_(H) gene segment is a human V_(H)1-2 gene segment and/or polymorphic variants thereof.

In one embodiment, the mouse further comprises a replacement at an endogenous immunoglobulin light chain locus of all or substantially all endogenous V_(L) gene segments with one or more human V_(L) gene segments. In a specific embodiment, the mouse further comprises one or more human J_(L) gene segments operably linked to the human V_(L) gene segments.

In one aspect, use of a mouse as described herein to make an immunoglobulin variable region nucleotide sequence is provided. In one embodiment, the sequence comprises a rearranged V_(H)1-69 gene segment. In one embodiment, the sequence comprises a rearranged V_(H)1-2 gene segment.

In one embodiment, the immunoglobulin variable region nucleotide sequence is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical with a human V_(H)1-69 gene segment. In a specific embodiment, the immunoglobulin variable region nucleotide sequence is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical with SEQ ID NO: 34. In various embodiments, the human V_(H)1-69 gene segment is identified from Table 2.

In one embodiment, the immunoglobulin variable region nucleotide sequence encodes an amino acid sequence that is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical with SEQ ID NO: 35.

In one embodiment, the immunoglobulin variable region nucleotide sequence is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical with a human V_(H)1-2 gene segment. In a specific embodiment, the immunoglobulin variable region nucleotide sequence is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical with SEQ ID NO: 60. In various embodiments, the human V_(H)1-2 gene segment is identified from Table 3.

In one embodiment, the immunoglobulin variable region nucleotide sequence encodes an amino acid sequence that is at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% identical with SEQ ID NO: 61.

In one aspect, use of a mouse as described herein to make a fully human Fab or a fully human F(ab)₂ is provided. In one embodiment, the fully human Fab or fully human F(ab)2 comprises a heavy chain variable region that comprises a rearranged human V_(H)1-69 gene segment. In one embodiment, the fully human Fab or fully human F(ab)2 comprises a heavy chain variable region that comprises a rearranged human V_(H)1-2 gene segment.

In one aspect, use of a mouse as described herein to make an immortalized cell line is provided.

In one aspect, use of a mouse as described herein to make a hybridoma or quadroma is provided.

In one aspect, use of a mouse as described herein to make a phage library containing human heavy chain variable regions and human light chain variable regions is provided.

In one embodiment, the human heavy chain variable regions are derived from a human V_(H)1-69 gene segment that comprises a sequence selected from SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56 and SEQ ID NO: 58.

In one embodiment, the human heavy chain variable regions are derived from a human V_(H)1-69 gene segment that comprises a sequence selected from SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41, SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51, SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57 and SEQ ID NO: 59.

In one embodiment, the human heavy chain variable regions are all derived from a human V_(H)1-2 gene segment that comprises a sequence selected from SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66 and SEQ ID NO: 68.

In one embodiment, the human heavy chain variable regions are derived from a human V_(H)1-2 gene segment that comprises a sequence selected from SEQ ID NO: 61, SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67 and SEQ ID NO: 69.

In one aspect, use of a mouse as described herein to generate a variable region sequence for making a human antibody is provided, comprising (a) immunizing a mouse as described herein with an antigen of interest, (b) isolating a lymphocyte from the immunized mouse of (a), (c) exposing the lymphocyte to one or more labeled antibodies, (d) identifying a lymphocyte that is capable of binding to the antigen of interest, and (e) amplifying one or more variable region nucleic acid sequence from the lymphocyte thereby generating a variable region sequence.

In one embodiment, the lymphocyte is derived or isolated from the spleen of the mouse. In one embodiment, the lymphocyte is derived or isolated from a lymph node of the mouse. In one embodiment, the lymphocyte is derived or isolated from the bone marrow of the mouse. In one embodiment, the lymphocyte is derived or isolated from the blood of the mouse.

In one embodiment, the labeled antibody is a fluorophore-conjugated antibody. In one embodiment, the one or more fluorophore-conjugated antibodies are selected from an IgM, an IgG, and/or a combination thereof.

In one embodiment, the lymphocyte is a B cell.

In one embodiment, the one or more variable region nucleic acid sequence comprises a heavy chain variable region sequence. In one embodiment, the one or more variable region nucleic acid sequence comprises a light chain variable region sequence. In a specific embodiment, the light chain variable region sequence is an immunoglobulin κ light chain variable region sequence. In one embodiment, the one or more variable region nucleic acid sequence comprises a heavy chain and a κ light chain variable region sequence.

In one embodiment, use of a mouse as described herein to generate a heavy and a κ light chain variable region sequence for making a human antibody is provided, comprising (a) immunizing a mouse as described herein with an antigen of interest, (b) isolating the spleen from the immunized mouse of (a), (c) exposing B lymphocytes from the spleen to one or more labeled antibodies, (d) identifying a B lymphocyte of (c) that is capable of binding to the antigen of interest, and (e) amplifying a heavy chain variable region nucleic acid sequence and a κ light chain variable region nucleic acid sequence from the B lymphocyte thereby generating the heavy chain and x light chain variable region sequences.

In one embodiment, use of a mouse as described herein to generate a heavy and a κ light chain variable region sequence for making a human antibody is provided, comprising (a) immunizing a mouse as described herein with an antigen of interest, (b) isolating one or more lymph nodes from the immunized mouse of (a), (c) exposing B lymphocytes from the one or more lymph nodes to one or more labeled antibodies, (d) identifying a B lymphocyte of (c) that is capable of binding to the antigen of interest, and (e) amplifying a heavy chain variable region nucleic acid sequence and a κ light chain variable region nucleic acid sequence from the B lymphocyte thereby generating the heavy chain and κ light chain variable region sequences.

In one embodiment, use of a mouse as described herein to generate a heavy and a κ light chain variable region sequence for making a human antibody is provided, comprising (a) immunizing a mouse as described herein with an antigen of interest, (b) isolating bone marrow from the immunized mouse of (a), (c) exposing B lymphocytes from the bone marrow to one or more labeled antibodies, (d) identifying a B lymphocyte of (c) that is capable of binding to the antigen of interest, and (e) amplifying a heavy chain variable region nucleic acid sequence and a κ light chain variable region nucleic acid sequence from the B lymphocyte thereby generating the heavy chain and κ light chain variable region sequences. In various embodiments, the one or more labeled antibodies are selected from an IgM, an IgG, and/or a combination thereof.

In various embodiments, the antigen of interest is a pathogen that afflicts human subjects including, e.g., a viral antigen. Exemplary viral pathogens include, e.g., mainly those of the families of Adenoviridae, bacteria Picornaviridae, Herpesviridae, Hepadnaviridae, Flaviviridae, Retroviridae, Orthomyxoviridae, Paramyxoviridae, Papovaviridae, Polyomavirus, Rhabdoviridae, and Togaviridae. Such exemplary viruses typically range between 20-300 nanometers in length. In various embodiments, the antigen of interest is a viral antigen selected from a hepatitis virus (e.g., HCV, HBV, etc.), a human immunodeficiency virus (HIV), or an influenza virus (e.g., H1N1).

In various embodiments, use of a mouse as described herein to generate a heavy and κ light chain variable region sequence for making a human antibody is provided, further comprising fusing the amplified heavy and light chain variable region sequences to human heavy and light chain constant region sequences, expressing the fused heavy and light chain sequences in a cell, and recovering the expressed heavy and light chain sequences thereby generating a human antibody.

In various embodiments, the human heavy chain constant regions are selected from IgM, IgD, IgA, IgE and IgG. In various specific embodiments, the IgG is selected from an IgG1, an IgG2, an IgG3 and an IgG4. In various embodiments, the human heavy chain constant region comprises a C_(H)1, a hinge, a C_(H)2, a C_(H)3, a C_(H)4, or a combination thereof. In various embodiments, the light chain constant region is an immunoglobulin κ constant region. In various embodiments, the cell is selected from a HeLa cell, a DU145 cell, a Lncap cell, a MCF-7 cell, a MDA-MB-438 cell, a PC3 cell, a T47D cell, a THP-1 cell, a U87 cell, a SHSY5Y (human neuroblastoma) cell, a Saos-2 cell, a Vero cell, a CHO cell, a GH3 cell, a PC12 cell, a human retinal cell (e.g., a PER.C6™ cell), and a MC3T3 cell. In a specific embodiment, the cell is a CHO cell.

In one aspect, a method for generating a reverse-chimeric rodent-human antibody specific against an antigen of interest is provided, comprising the steps of immunizing a mouse as described herein with the antigen, isolating at least one cell from the mouse producing a reverse-chimeric mouse-human antibody specific against the antigen, culturing at least one cell producing the reverse-chimeric mouse-human antibody specific against the antigen, and obtaining said antibody.

In one embodiment, the reverse-chimeric mouse-human antibody comprises a human heavy chain variable domain fused with a mouse or rat heavy chain constant gene, and a human light chain variable domain fused with a mouse or rat or human light chain constant gene. In a specific embodiment, the human heavy chain variable domain contains a rearranged human V_(H)1-69 or human V_(H)1-2 gene segment.

In one embodiment, culturing at least one cell producing the reverse-chimeric rodent-human antibody specific against the antigen is performed on at least one hybridoma cell generated from the at least one cell isolated from the mouse.

In one embodiment, the antigen of interest is a pathogen that afflicts human subjects as described herein.

In one aspect, a method for generating a fully human antibody specific against an antigen of interest is provided, comprising the steps of immunizing a mouse as described herein with the antigen, isolating at least one cell from the mouse producing a reverse-chimeric rodent-human antibody specific against the antigen, generating at least one cell producing a fully human antibody derived from the reverse-chimeric rodent-human antibody specific against the antigen, and culturing at least one cell producing the fully human antibody, and obtaining said fully human antibody.

In various embodiments, the at least one cell isolated from the mouse producing a reverse-chimeric rodent-human antibody specific against the antigen is a splenocyte or a B cell.

In various embodiments, the antibody is a monoclonal antibody.

In various embodiments, the antibody comprises a heavy chain variable domain that contains a rearranged human V_(H)1-69 or human V_(H)1-2 gene segment.

In various embodiments, immunization with the antigen of interest is carried out with protein, DNA, a combination of DNA and protein, or cells expressing the antigen. In one embodiment, the antigen of interest is a pathogen that afflicts human subjects as described herein.

In one aspect, use of a mouse as described herein to make a nucleic acid sequence encoding an immunoglobulin variable region or fragment thereof is provided. In one embodiment, the nucleic acid sequence is used to make a human antibody or antigen-binding fragment thereof. In one embodiment, the mouse is used to make an antigen-binding protein selected from an antibody, a multi-specific antibody (e.g., a bi-specific antibody), an scFv, a bi-specific scFv, a diabody, a triabody, a tetrabody, a V-NAR, a V_(HH), a V_(L), a F(ab), a F(ab)₂, a DVD (i.e., dual variable domain antigen-binding protein), a an SVD (i.e., single variable domain antigen-binding protein), or a bispecific T-cell engager (BiTE).

In one aspect, a method for making a human antigen-binding protein is provided, comprising exposing a genetically modified non-human animal as described herein to an antigen of interest, allowing the genetically modified non-human animal to mount an immune response to the antigen, obtaining from the genetically modified non-human animal a heavy chain variable domain nucleic acid sequence encoding a human heavy chain variable domain that specifically binds the antigen of interest, cloning the heavy chain variable domain nucleic acid sequence to a human constant region sequence, and expressing in a mammalian cell an antibody comprising the human heavy chain variable domain sequence and the human constant region sequence. In one embodiment, the mammalian cell is a CHO cell. In one embodiment the genetically modified non-human animal comprises a human V_(H) gene segment repertoire that consists essentially of a single human V_(H) gene segment, optionally present in two or more polymorphic variants thereof, operably linked to one or more human D and/or J segments. In one embodiment, the human V_(H) gene segment repertoire is at an endogenous non-human V_(H) segment locus. In one embodiment, the human V_(H) gene segment repertoire is at a locus that is not an endogenous V_(H) segment locus. In one embodiment, the human V_(H) gene segment rearranges with a human D segment and a human J segment to form a rearranged human VDJ gene operably linked to a constant region sequence, wherein the constant region sequence is selected from a human sequence and a rodent sequence (e.g., a mouse or rat or hamster sequence). In one embodiment, the constant region sequence comprises a sequence selected from a C_(H)1, a hinge, a C_(H)2, a C_(H)3, and a combination thereof; in a specific embodiment, the constant region sequence comprises a C_(H)1, a hinge, a C_(H)2, and a C_(H)3. In one embodiment, the human variable domain and the constant sequence are expressed in the mammalian cell with a cognate human light chain variable domain obtained from the same mouse (e.g., sequence obtained from the same B cell as the human variable domain sequence); in one embodiment the sequence encoding the human light chain variable domain obtained from the mouse is then fused with a sequence encoding a human light chain constant sequence, and the light chain sequence and the heavy chain sequence are expressed in the mammalian cell.

In one embodiment, the antigen of interest is a pathogen that afflicts human subjects as described herein.

In one aspect, a method for making an antibody heavy chain variable domain that binds an antigen of interest is provided, comprising expressing in a single cell (a) a first V_(H) sequence of an immunized non-human animal as described herein, wherein the first V_(H) sequence is fused with a C_(H) gene sequence; and (b) a V_(L) gene sequence of an immunized non-human animal as described herein, wherein the V_(L) gene sequence is fused with a human C_(L) gene sequence; maintaining the cell under conditions sufficient to express an antibody; and, isolating the antibody heavy chain variable domain. In one embodiment, the V_(L) gene sequence is cognate with the first V_(H) sequence.

In one embodiment, the cell comprises a second V_(H) gene sequence of an immunized non-human animal as described herein, wherein the second V_(H) gene sequence is fused with a C_(H) gene sequence, wherein the first V_(H) gene sequence encodes a V_(H) domain that specifically binds a first epitope, and the second V_(H) gene sequence encodes a V_(H) domain that specifically binds a second epitope, wherein the first epitope and the second epitope are not identical.

In one embodiment, the constant region sequences are all human constant region sequences. In one embodiment, the antigen of interest is a pathogen that afflicts human subjects as described herein.

In one aspect, a method for making a human bispecific antibody is provided, comprising making the bispecific antibody using human variable region gene sequences of B cells of a non-human animal as described herein.

In one embodiment, the method comprises (a) identifying a clonally selected lymphocyte of the non-human animal, wherein the non-human animal has been exposed to an antigen of interest and allowed to develop an immune response to the antigen of interest, and wherein the lymphocyte expresses an antibody that specifically binds the antigen of interest, (b) obtaining from the lymphocyte or the antibody a nucleotide sequence that encodes a human heavy chain variable region that specifically binds the antigen of interest, and (c) employing the nucleotide sequence that encodes the human heavy chain variable region that specifically binds the antigen of interest in making the bispecific antibody. In a specific embodiment, the human heavy chain variable region comprises a rearranged V_(H)1-2 or V_(H)1-69 gene segment.

In one embodiment, steps (a) through (c) are performed a first time for a first antigen of interest to generate a first human heavy chain variable region sequence, and steps (a) through (c) are performed a second time for a second antigen of interest to generate a second human heavy chain variable region sequence, and wherein the first human heavy chain variable region sequence is expressed fused with a first human heavy chain constant region to form a first human heavy chain, the second human heavy chain variable region sequence is expressed fused with a second human heavy chain constant region to form a second human heavy chain, wherein the first and the second human heavy chains are expressed in the presence of a single human light chain expressed from a rearranged human V_(κ)1-39 or a human V_(κ)3-20 gene segment. In a specific embodiment, the single human light chain comprises a germline sequence.

In one embodiment, the method comprises (a) cloning heavy chain variable regions from B cells of a non-human animal as described herein which has been exposed to a first antigen of interest, and the same non-human animal, or a different non-human animal which is genetically the same and has been exposed to a second antigen of interest; and (b) expressing in a cell the heavy chain variable regions of (a) with the same heavy chain constant region and the same light chain to make a bispecific antibody.

In one aspect, a use of a non-human animal as described herein is provided, to obtain a nucleic acid sequence that encodes a human heavy chain variable domain. In one embodiment, the heavy chain variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2 and V_(H)1-69.

In one aspect, a use of a non-human animal as described herein is provided, to obtain a cell that encodes a human heavy chain variable domain. In one embodiment, the heavy chain variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2 and V_(H)1-69.

In one aspect, use of a non-human animal as described herein to make a human antibody variable domain is provided. In one embodiment, the variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2 and V_(H)1-69.

In one aspect, use of a non-human animal as described herein to make a human antibody is provided, comprising making the antibody using human variable region gene sequences of B cells of a non-human animal as described herein. In one embodiment, the human antibody is a human bispecific antibody. In a specific embodiment, the bispecific antibody comprises one heavy chain variable domain derived from a rearranged human V_(H)1-2 or V_(H)1-69 gene segment. In one embodiment, the human variable region gene sequences comprise a rearranged human V_(H)1-2 or V_(H)1-69 gene segment.

In one aspect, use of a non-human animal as described herein is provided to select a human immunoglobulin heavy chain variable domain. In one embodiment, the heavy chain variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2 and V_(H)1 -69.

In one aspect, use of the mouse as described herein for the manufacture of a medicament (e.g., an antigen-binding protein), or for the manufacture of a sequence encoding a variable sequence of a medicament (e.g., an antigen-binding protein), for the treatment of a human disease or disorder is provided. In one embodiment, the variable sequence of a medicament comprises a polymorphic human V_(H) gene segment. In one embodiment, the variable sequence of a medicament comprises a human V_(H)1-69 gene segment. In one embodiment, the variable sequence of a medicament comprises a human V_(H)1-2 gene segment.

In one aspect, a nucleic acid construct encoding an immunoglobulin variable domain made in a mouse as described herein is provided. In one embodiment, the variable domain is a heavy chain variable domain. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, or V_(H)3-23. In another specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H)1-2 gene segment. In another specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H)1-69 gene segment.

In one embodiment, the variable domain is a light chain variable domain. In a specific embodiment, the variable domain is a κ light chain variable domain that is cognate with a human heavy chain variable domain that comprises a rearranged human V_(H)1-69 gene segment. In a specific embodiment, the variable domain is a κ light chain variable domain that is cognate with a human heavy chain variable domain that comprises a rearranged human V_(H)1-2 gene segment.

In one aspect, use of a mouse as described herein to make a nucleic acid construct encoding a human immunoglobulin variable domain is provided. In one embodiment, the variable domain is a light chain variable domain. In one embodiment, the variable domain is a κ light chain variable domain that comprises a rearranged human V_(κ) gene segment selected from V_(κ)4-1, V_(κ)5-2, V_(κ)7-3, V_(κ)2-4, V_(κ)1-5, V_(κ)1-6, V_(κ)3-7, V_(κ)1-8, V_(κ)1-9, V_(κ)2-10, V_(κ)3-11, V_(κ)1-12, V_(κ)1-13, V_(κ)2-14, V_(κ)3-15, V_(κ)1-16, V_(κ)1-17, V_(κ)2-18, V_(κ)2-19, V_(κ)3-20, V_(κ)6-21, V_(κ)1-22, V_(κ)1-23, V_(κ)2-24, V_(κ)3-25, V_(κ)2-26, V_(κ)1-27, V_(κ)2-28, V_(κ)2-29, V_(κ)2-30, V_(κ)3-31, V_(κ)1-32, V_(κ)1-33, V_(κ)3-34, V_(κ)1-35, V_(κ)2-36, V_(κ)1-37, V_(κ)2-38, V_(κ)1-39, and V_(κ)2-40.

In one embodiment, the variable domain is a heavy chain variable domain. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, or V_(H)3-23. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H)1-69 gene segment. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H)1-2 gene segment.

In one aspect, use of a mouse as described herein to make a human immunoglobulin variable domain is provided. In one embodiment, the variable domain is a light chain variable domain. In one embodiment, the variable domain is a κ light chain variable domain that comprises a rearranged human V_(κ) gene segment selected from V_(κ)4-1, V_(κ)5-2, V_(κ)7-3, V_(κ)2-4, V_(κ)1-5, V_(κ)1-6, V_(κ)3-7, V_(κ)1-8, V_(κ)1-9, V_(κ)2-10, V_(κ)3-11, V_(κ)1-12, V_(κ)1-13, V_(κ)2-14, V_(κ)3-15, V_(κ)1-16, V_(κ)1-17, V_(κ)2-18, V_(κ)2-19, V_(κ)3-20, V_(κ)6-21, V_(κ)1-22, V_(κ)1-23, V_(κ)2-24, V_(κ)3-25, V_(κ)2-26, V_(κ)1-27, V_(κ)2-28, V_(κ)2-29, V_(κ)2-30, V_(κ)3-31, V_(κ)1-32, V_(κ)1-33, V_(κ)3-34, V_(κ)1-35, V_(κ)2-36, V_(κ)1-37, V_(κ)2-38, V_(κ)1-39, and V_(κ)2-40.

In one embodiment, the variable domain is a heavy chain variable domain. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H) gene segment selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, or V_(H)3-23. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H)1-69 gene segment. In a specific embodiment, the heavy chain variable domain comprises a rearranged human V_(H)1-2 gene segment.

In one aspect, use of a non-human animal as described herein to make a nucleic acid sequence encoding a human heavy chain variable domain is provided. In one embodiment, the human heavy chain variable domain is characterized by having human FR1-CDR1-FR2-CDR2-FR3 sequences that are derived from a polymorphic human V_(H) gene segment. In a specific embodiment, the human V_(H) gene segment is selected from a human V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, or V_(H)3-23 gene segment. In one embodiment, the human V_(H) gene segment is a human V_(H)1-69 gene segment. In one embodiment, the human V_(H) gene segment is a human V_(H)1-2 gene segment.

In one aspect, a method for making a nucleic acid sequence encoding a human V_(H) domain is provided, the method comprising immunizing a non-human animal as described herein with an antigen of interest, allowing the non-human animal to mount an immune response to the antigen of interest, and obtaining therefrom a nucleic acid sequence encoding a human V_(H) domain that binds the antigen of interest. In one embodiment, the method further comprises making a nucleic acid sequence encoding a human V_(L) domain that is cognate with the human V_(H) domain, comprising isolating a B cell encoding the human V_(H) domain and the human V_(L) domain, and obtaining therefrom the sequence of the heavy and light chain variable domains. In various embodiments, the human V_(H) domain is derived from a rearranged human V_(H)1-69 or human V_(H)1-2 gene segment. In various embodiments, the human V_(L) domain is selected from a human V_(κ) or a human V_(λ) domain.

In one aspect, use of a non-human animal as described herein to make a human therapeutic is provided, comprising immunizing the non-human animal with an antigen of interest, allowing the non-human animal to mount an immune response, and obtaining from the animal a nucleic acid sequence encoding an immunoglobulin variable domain that binds the antigen of interest, and employing the immunoglobulin variable domain in a human therapeutic. In one embodiment, the variable domain is a heavy chain variable domain. In a specific embodiment, the heavy chain variable domain is derived from a rearranged human V_(H)1-69 or a human V_(H)1-2 gene segment. In one embodiment, the variable domain is a light chain variable domain. In a specific embodiment, the light chain variable domain is derived from a rearranged human V_(κ) or human V_(λ) gene segment.

In one aspect, a method for making a human therapeutic is provided, comprising immunizing a non-human animal as described herein with an antigen of interest, allowing the non-human animal to mount an immune response, and obtaining from the animal a nucleic acid sequence encoding an immunoglobulin variable domain that binds the antigen of interest, and employing the immunoglobulin variable domain in a human therapeutic. In one embodiment, the variable domain is a heavy chain variable domain. In a specific embodiment, the heavy chain variable domain is derived from a rearranged human V_(H)1-69 or a human V_(H)1-2 gene segment. In one embodiment, the variable domain is a light chain variable domain. In a specific embodiment, the light chain variable domain is derived from a rearranged human V_(κ) or human V_(λ) gene segment.

In one aspect, a method for making a human antigen-binding protein is provided, comprising immunizing a non-human animal as described herein with an antigen of interest, allowing the animal to mount an immune response, obtaining from the mouse a nucleic acid sequence encoding an immunoglobulin variable domain that specifically binds the antigen of interest, cloning the nucleic acid sequence in a vector suitable for expression of the nucleic acid, wherein the nucleic acid sequence is cloned in frame with a nucleic acid sequence encoding a human immunoglobulin constant region or functional fragment thereof, and inserting the vector in a mammalian cell, and maintaining the cell under conditions suitable for expressing an antigen-binding protein that comprises the immunoglobulin variable domain and the immunoglobulin constant region or functional fragment thereof. In one embodiment, the antigen-binding protein is a human antibody. In a specific embodiment, the antibody comprises a heavy chain variable domain and a light chain variable domain obtained from a mouse as described herein. In a specific embodiment, the antibody comprises a heavy chain variable domain obtained from a mouse as described herein. In various embodiments, the heavy chain variable domain is derived from a rearranged human V_(H)1-69 or a human V_(H)1-2 gene segment.

In one aspect, a nucleic acid sequence encoding a human antigen-binding domain made in a non-human animal as described herein is provided. In one embodiment, the nucleic acid sequence encodes a human immunoglobulin V_(H) domain. In one embodiment, the nucleic acid sequence encodes a human immunoglobulin V_(H) domain and a cognate human V_(L) domain. In various embodiments, the human V_(H) domain is derived from a rearranged human V_(H)1-69 or a human V_(H)1-2 gene segment.

In one aspect, a method for preparation of a human antibody is provided, comprising immunizing a non-human animal as described herein with an antigen of interest, allowing the non-human animal to mount an immune response, harvesting a lymphocyte (e.g., a B cell) from the immunized animal, fusing the lymphocyte with a myeloma cell to form a hybridoma cell, obtaining from the hybridoma cell a nucleic acid sequence that encodes a human V_(H) domain and a human V_(L) domain, cloning the nucleic acid sequence in frame (i.e., in operable linkage) with a human constant region sequence to create an immunoglobulin heavy chain and an immunoglobulin light chain, and expressing the heavy and light chains in a cell capable of expressing the fully human antibody. In one embodiment, the cell is a CHO cell. In various embodiments, the human V_(H) domain is derived from a rearranged human V_(H)1-69 gene segment or a human V_(H)1-2 gene segment.

In one aspect, a method for preparation of a human antibody is provided, comprising immunizing a non-human animal as described herein with an antigen of interest, allowing the non-human animal to mount an immune response, harvesting a lymphocyte (e.g., a B cell) from the immunized animal, obtaining from the lymphocyte a nucleic acid sequence that encodes a human V_(H) domain and a human V_(L) domain, cloning the nucleic acid sequence in frame (i.e., in operable linkage) with a human constant region sequence to create an immunoglobulin heavy chain and an immunoglobulin light chain, and expressing the heavy and light chains in a cell capable of expressing the fully human antibody. In one embodiment, the lymphocyte is derived from the spleen of the non-human animal. In one embodiment, the cell is a CHO cell. In various embodiments, the human V_(H) domain is derived from a rearranged human V_(H)1-69 gene segment or a human V_(H)1-2 gene segment.

In various aspects, the antigen of interest is a pathogen that afflicts human subjects as described herein. In various aspects, the antigen of interest is a virus that is capable of infecting a human. Exemplary antigens that can be employed in the methods and uses described herein include microbes or microorganisms such as a virus, bacterium, prion, or fungus or any other pathogen that causes disease in humans. A person of skill, upon reading the disclosure, will appreciate those human pathogens that will be applicable for the methods and uses described herein. The various aspects and embodiments are capable of use together, unless expressly noted otherwise or the context clearly prohibits use together.

BRIEF DESCRIPTION OF FIGURES

FIG. 1 shows a general illustration, not to scale, of a series of targeting and molecular engineering steps employed to make a targeting vector for construction of a modified heavy chain locus containing a single human V_(H)1-69 gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at an endogenous immunoglobulin heavy chain locus.

FIG. 2 shows a general illustration, not to scale, of a series of targeting and molecular engineering steps employed to make a targeting vector for construction of a modified heavy chain locus containing a single human V_(H)1-2 gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at an endogenous immunoglobulin heavy chain locus.

FIG. 3 shows contour plots of splenocytes gated on single lymphocytes and stained for CD19 (B cell) and CD3 (T cell) from a wild type mouse (WT) and a mouse homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 4A shows, on the left, the percent of CD19⁺ B cells in spleens harvested from wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO). On the right, the number of CD19⁺ B cells per spleen is shown for both wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 4B shows, on the left, the percent of CD19⁺ B cells in bone marrow harvested from femurs of wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO). On the right, the number of CD19⁺ B cells per femur is shown for both wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 5 shows contour plots of splenocytes gated on CD19⁺ B cells and stained for Igλ+ and Igκ+ expression from a wild type mouse (WT) and a mouse homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 6 shows contour plots of splenocytes gated on CD19⁺ B cells and stained for immunoglobulin D (IgD) and immunoglobulin M (IgM) from a wild type mouse (WT) and a mouse homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 7 shows the total number of transitional B cells (CD19⁺IgM^(hi)IgD^(int)), mature B cells (CD19⁺IgM^(int)IgD^(hi)), and the ratio of mature to immature B cells in harvested spleens from wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 8 shows contour plots of bone marrow gated on singlets stained for immunoglobulin M (IgM) and B220 from a wild type mouse (WT) and a mouse homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 9 shows the total number of immature (B220^(int)IgM⁺) and mature (B220^(hi)IgM⁺) B cells in bone marrow isolated from the femurs of wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 10 shows contour plots of bone marrow gated on CD19⁺ B cells and stained for ckit⁺ and CD43⁺ from a wild type mouse (WT) and a mouse homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 11A shows the percent of CD19⁺ cells in populations of pro B (CD19⁺CD43⁺ckit⁺) and pre B (CD19⁺CD43⁻ckit⁻) cells in bone marrow harvested from the femurs of wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 11B shows the absolute number of cells per femur in populations of pro B (CD19⁺CD43⁺ckit⁺) and pre B (CD19⁺CD43⁻ckit⁻) cells in bone marrow harvested from wild type mice (WT) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO).

FIG. 12 shows the relative mRNA expression (y-axis) in purified splenic B cells of V_(H)1-69-derived heavy chains in a quantitative PCR assay using a probe specific for the human V_(H)1-69 gene segment in mice homozygous for a replacement of the endogenous heavy chain V_(H), D_(H), J_(H), and a replacement of the endogenous light chain V_(κ) and J_(κ) gene segments with human V_(H), D_(H), J_(H), V_(κ) and J_(κ) gene segments (HK), wild type mice (WT), mice heterozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HET) and mice homozygous for a single human V_(H) gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H) HO). Signals are normalized to expression of mouse C_(κ).

FIG. 13 shows the nucleotide alignment of the second exon for each of thirteen reported alleles for the human V_(H)1-69 gene. Lower case bases indicate germline nucleotide differences among the alleles. Complementary determining regions (CDRs) are indicated with boxes around the sequence. Dashes indicate artificial gaps for proper sequence alignment. V_(H)1-69*01 (SEQ ID NO: 34); V_(H)1-69*02 (SEQ ID NO: 36); V_(H)1-69*03 (SEQ ID NO: 38); V_(H)1-69*04 (SEQ ID NO: 40); V_(H)1-69*05 (SEQ ID NO: 42); V_(H)1-69*06 (SEQ ID NO: 44); V_(H)1-69*07 (SEQ ID NO: 46); V_(H)1-69*08 (SEQ ID NO: 48); V_(H)1-69*09 (SEQ ID NO: 50); V_(H)1-69*10 (SEQ ID NO: 52); V_(H)1-69*11 (SEQ ID NO: 54); V_(H)1-69*12 (SEQ ID NO: 56); V_(H)1-69*13 (SEQ ID NO: 58).

FIG. 14 shows the protein alignment of the mature heavy chain variable gene sequence for each of thirteen reported alleles for the human V_(H)1-69 gene. Lower case amino acids indicate germline differences among the alleles. Complementary determining regions (CDRs) are indicated with boxes around the sequence. Dashes indicate artificial gaps for proper sequence alignment. V_(H)1-69*01 (SEQ ID NO: 35); V_(H)1-69*02 (SEQ ID NO: 37); V_(H)1-69*03 (SEQ ID NO: 39); V_(H)1-69*04 (SEQ ID NO: 41); V_(H)1-69*05 (SEQ ID NO: 43); V_(H)1-69*06 (SEQ ID NO: 45); V_(H)1-69*07 (SEQ ID NO: 47); V_(H)1-69*08 (SEQ ID NO: 49); V_(H)1-69*09 (SEQ ID NO: 51); V_(H)1-69*10 (SEQ ID NO: 53); V_(H)1-69*11 (SEQ ID NO: 55); V_(H)1-69*12 (SEQ ID NO: 57); V_(H)1-69*13 (SEQ ID NO: 59).

FIG. 15 shows a percent identity/percent similarity matrix for the aligned protein sequences of the mature variable gene for each of thirteen reported alleles for the human V_(H)1-69 gene. Percent identity among the V_(H)1-69 alleles is indicated above the shaded boxes and percent similarity is indicated below the shaded boxes. Scores for percent identity and percent similarity were scored by a ClustalW (v1.83) alignment tool using MacVector software (MacVector, Inc., North Carolina).

FIG. 16 shows the nucleotide alignment of the second exon for each of five reported alleles for the human V_(H)1-2 gene. Lower case bases indicate germline nucleotide differences among the alleles. Complementary determining regions (CDRs) are indicated with boxes around the sequence. Dashes indicate artificial gaps for proper sequence alignment. V_(H)1-2*01 (SEQ ID NO: 60); V_(H)1-2*02 (SEQ ID NO: 62); V_(H)1-2*03 (SEQ ID NO: 64); V_(H)1-2*04 (SEQ ID NO: 66); V_(H)1-2*05 (SEQ ID NO: 68).

FIG. 17 shows the protein alignment of the mature heavy chain variable gene sequence for each of five reported alleles for the human V_(H)1-2 gene. Lower case amino acids indicate germline differences among the alleles. Complementary determining regions (CDRs) are indicated with boxes around the sequence. Dashes indicate artificial gaps for proper sequence alignment. V_(H)1-2*01 (SEQ ID NO: 61); V_(H)1-2*02 (SEQ ID NO: 63); V_(H)1-2*03 (SEQ ID NO: 65); V_(H)1-2*04 (SEQ ID NO: 67); V_(H)1-2*05 (SEQ ID NO: 69).

FIG. 18 shows a percent identity/percent similarity matrix for the aligned protein sequences of the mature variable gene for each of five reported alleles for the human V_(H)1-2 gene. Percent identity among the V_(H)1-2 alleles is indicated above the shaded boxes and percent similarity is indicated below the shaded boxes. Scores for percent identity and percent similarity were scored by a ClustalW (v1.83) alignment tool using MacVector software (MacVector, Inc., North Carolina).

FIG. 19 shows the antibody titer from mice homozygous for human heavy and human κ light chain variable gene loci (H_(κ); n=4) and mice homozygous for a single human V_(H)1-69 gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H)HO; n=10) that were immunized with a human cell surface receptor (Antigen A).

FIG. 20 shows the antibody titer from mice homozygous for human heavy and human κ light chain variable gene loci (H_(κ); n=5) and mice homozygous for a single human V_(H)1-69 gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus (1hV_(H)HO; n=5) that were immunized with two different influenza vaccines.

FIG. 21 shows the percentage (y-axis) of IgM-primed heavy chains having a specified amino acid length for the V_(H) CDR3 region (x-axis) from mice homozygous for a single human V_(H)1-69 gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus and homozygous for a replacement of the endogenous κ light chain variable loci with human κ light chain variable loci that were immunized with a human cell surface receptor (Antigen A).

FIG. 22 shows the percentage (y-axis) of IgG-primed heavy chains having a specified amino acid length for the V_(H) CDR3 region (x-axis) from mice homozygous for a single human V_(H)1-69 gene segment, twenty-seven human D_(H) and six human J_(H) gene segments at the endogenous immunoglobulin heavy chain locus and homozygous for a replacement of the endogenous κ light chain variable loci with human κ light chain variable loci that were immunized with a human cell surface receptor (Antigen A).

DETAILED DESCRIPTION

This invention is not limited to particular methods, and experimental conditions described, as such methods and conditions may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present invention is defined by the claims.

Unless defined otherwise, all terms and phrases used herein include the meanings that the terms and phrases have attained in the art, unless the contrary is clearly indicated or clearly apparent from the context in which the term or phrase is used. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, particular methods and materials are now described. All publications mentioned are hereby incorporated by reference.

The phrase “substantial” or “substantially” when used to refer to an amount of gene segments (e.g., “substantially all” V gene segments) includes both functional and non functional gene segments and include, in various embodiments, e.g., 80% or more, 85% or more, 90% or more, 95% or more 96% or more, 97% or more, 98% or more, or 99% or more of all gene segments; in various embodiments, “substantially all” gene segments includes, e.g., at least 95%, 96%, 97%, 98%, or 99% of functional (i.e., non-pseudogene) gene segments.

The term “replacement” includes wherein a DNA sequence is placed into a genome of a cell in such a way as to replace a sequence within the genome with a heterologous sequence (e.g., a human sequence in a mouse), at the locus of the genomic sequence. The DNA sequence so placed may include one or more regulatory sequences that are part of source DNA used to obtain the sequence so placed (e.g., promoters, enhancers, 5′- or 3′-untranslated regions, appropriate recombination signal sequences, etc.). For example, in various embodiments, the replacement is a substitution of an endogenous sequence for a heterologous sequence that results in the production of a gene product from the DNA sequence so placed (comprising the heterologous sequence), but not expression of the endogenous sequence; the replacement is of an endogenous genomic sequence with a DNA sequence that encodes a protein that has a similar function as a protein encoded by the endogenous genomic sequence (e.g., the endogenous genomic sequence encodes an immunoglobulin gene or domain, and the DNA fragment encodes one or more human immunoglobulin genes or domains). In various embodiments, an endogenous gene or fragment thereof is replaced with a corresponding human gene or fragment thereof. A corresponding human gene or fragment thereof is a human gene or fragment that is an ortholog of, a homolog of, or is substantially identical or the same in structure and/or function, as the endogenous gene or fragment thereof that is replaced.

A precise, in situ replacement of six megabases of the variable regions of the mouse heavy chain immunoglobulin loci (V_(H)-D_(H)-J_(H)) with a restricted human immunoglobulin heavy chain locus was performed, while leaving the flanking mouse sequences intact and functional within the hybrid loci, including all mouse constant chain genes and locus transcriptional control regions (FIG. 1 and FIG. 2). Specifically, a single human V_(H), 27 D_(H), and six JH gene segments were introduced through chimeric BAC targeting vectors into mouse ES cells using VELOCIGENE® genetic engineering technology (see, e.g., U.S. Pat. No. 6,586,251 and Valenzuela et al., 2003, High-throughput engineering of the mouse genome coupled with high-resolution expression analysis, Nat Biotechnol 21:652-659).

Non-Human Animals With Restricted Immunoglobulin V_(H) Gene Segments

Non-human animals comprising immunoglobulin loci that comprise a restricted number of V_(H) genes, and one or more D genes and one or more J genes, are provided, as are methods of making and using them. When immunized with an antigen of interest, the non-human animals generate B cell populations with antibody variable regions derived only from the restricted, pre-selected V_(H) gene or set of V_(H) genes (e.g., a pre-selected V_(H) gene and variants thereof). In various embodiments, non-human animals are provided that generate B cell populations that express human antibody variable domains that are human heavy chain variable domains, along with cognate human light chain variable domains. In various embodiments, the non-human animals rearrange human heavy chain variable gene segments and human light chain variable gene segments from modified endogenous mouse immunoglobulin loci that comprise a replacement or insertion of the non-human unrearranged variable region sequences with human unrearranged variable region sequences.

Early work on the organization, structure, and function of the immunoglobulin genes was done in part on mice with disabled endogenous loci and engineered to have transgenic loci (randomly placed) with partial human immunoglobulin genes, e.g., a partial repertoire of human heavy chain genes linked with a human constant gene, randomly inserted into the genome, in the presence or absence of a human light chain transgene. Although these mice were somewhat less than optimal for making useful high affinity antibodies, they facilitated certain functional analyses of immunoglobulin loci. Some of these mice had as few as two or three, or even just a single, heavy chain variable gene.

Mice that express fully human immunoglobulin heavy chains derived from a single human V_(H)5-51 gene and 10 human D_(H) genes and six human J_(H) genes, with human μ and γ1 constant genes, on a randomly inserted transgene (and disabled endogenous immunoglobulin loci) have been reported (Xu and Davis, 2000, Diversity in the CDR3 Region of V_(H) Is Sufficient for Most Antibody Specificities, Immunity 13:37-45). The fully human immunoglobulin heavy chains of these mice are mostly expressed with one of just two fully mouse λ light chains derived from the endogenous mouse λ light chain locus (V_(λ)1-J_(λ)1 or V_(λ)2-J_(λ)2 only), and can express no κ light chain (the mice are Igλ^(−/−)). These mice exhibit severely abnormal dysfunction in B cell development and antibody expression. B cell numbers are reportedly 5-10% of wild-type, IgM levels 5-10% of wild-type, and IgG1 levels are only 0.1-1% of wild-type. The observed IgM repertoire revealed highly restricted junctional diversity. The fully human heavy chains display largely identical CDR3 length across antigens, the same J_(H) (J_(H)2) usage across antigens, and an initial junctional Q residue, thus reflecting a certain lack of CDR3 diversity. The fully mouse λ light chains nearly all had a W96L substitution in J_(λ)1 as initial junctional residue. The mice are reportedly unable to generate any antibodies against bacterial polysaccharide. Because the human variable domains couple with mouse light chains, the utility of the human variable regions is highly limited.

Other mice that have just a single human V_(H)3-23 gene, human D_(H) and J_(H) genes, and mouse light chain genes have been reported, but they exhibit a limited diversity (and thus a limited usefulness) due in part to mispairing potential between human V_(H) and mouse V_(L) domains (see, e.g., Mageed et al., 2001, Rearrangement of the human heavy chain variable region gene V3-23 in transgenic mice generates antibodies reactive with a range of antigens on the basis of V_(H)CDR3 and residues intrinsic to the heavy chain variable region, Clin. Exp. Immunol. 123:1-5). Similarly, mice that bear two V_(H) genes (3-23 and 6-1) along with human D_(H) and J_(H) genes in a transgene containing the human μ constant gene (Bruggemann et al., 1991, Human antibody production in transgenic mice: expression from 100 kb of the human IgH locus, Eur. J. Immmunol. 21:1323-1326) and express them in human IgM chains with mouse light chains may exhibit a repertoire limited by mispairing (Mackworth-Young et al., 2003, The role of antigen in the selection of the human V3-23 immunoglobulin heavy chain variable region gene, Clin. Exp. Immunol. 134:420-425).

Other transgenic mice that express V_(H)-restricted fully human heavy chains from a human transgene randomly inserted in the genome, with a limited human λ repertoire expressed from a fully human randomly inserted transgene, have also been reported (see, e.g., Taylor et al., 1992, A transgenic mouse that expresses a diversity of human sequence heavy and light chain immunoglobulins, Nucleic Acids Res. 20 (23):6287-6295; Wagner et al., 1994, Antibodies generated form human immunoglobulin miniloci in transgenic mice, Nucleic Acids Res. 22 (8):1389-1393). However, transgenic mice that express fully human antibodies from transgenes randomly integrated into the mouse genome, and that comprise damaged endogenous loci, are known to exhibit substantial differences in immune response as compared with wild-type mice that affect the diversity of the antibody variable domains obtainable from such mice.

Useful non-human animals that generate a diverse population of B cells that express human antibody variable domains from a restricted V_(H) gene repertoire and one or more D genes and one or more J genes will be capable of generating, preferably in some embodiments, repertoires of rearranged variable region genes that will be sufficiently diverse. In various embodiments, diversity includes junctional diversity, somatic hypermutation, and polymorphic diversity in V_(H) gene sequence (for embodiments where V_(H) genes are present in polymorphic forms). Combinatorial diversity occurs in the pairing of the V_(H) gene with one of a plurality of cognate human light chain variable domains (which, in various embodiments, comprise junctional diversity and/or somatic hypermutations).

Non-human animals comprising a restricted human V_(H) gene repertoire and a complete or substantially complete human V_(L) gene repertoire will in various embodiments generate populations of B cells that reflect the various sources of diversity, such as junctional diversity (e.g., VDJ, VJ joining, P additions, N additions), combinatorial diversity (e.g., cognate V_(H)-restricted human heavy, human light), and somatic hypermutations. In embodiments comprising a restriction of the V_(H) repertoire to one human V_(H) gene, the one human V_(H) gene can be present in two or more variants. In various embodiments, the presence of two or more polymorphic forms of a V_(H) gene will enrich the diversity of the variable domains of the B cell population.

Variations in the germline sequences of gene segments (e.g., V genes) contribute to the diversity of the antibody response in humans. The relative contribution to diversity due to V gene sequence differences varies among V genes. The degree of polymorphism varies across gene families, and is reflected in a plurality of haplotypes (stretches of sequence with coinherited polymorphisms) capable of generating further diversity as observed in V_(H) haplotype differences between related and unrelated individuals in the human population (see, e.g., Souroujon et al., 1989, Polymorphisms in Human H Chain V Region Genes from the V_(H)III Gene Family, J. Immunol. 143 (2):706-711). Some have suggested, based on data from particularly polymorphic human V_(H) gene families, that haplotype diversity in the germline is a major contributor to V_(H) gene heterogeneity in the human population, which is reflected in the large diversity of different germline V_(H) genes across the human population (see, Sasso et al., 1990, Prevalence and Polymorphism of Human V_(H)3 Genes, J. Immunol. 145 (8):2751-2757).

Although the human population displays a large diversity of haplotypes with respect to the V_(H) gene repertoire due to widespread polymorphism, certain polymorphisms are reflected in prevalent (i.e., conserved) alleles observed in the human population (Sasso et al., 1990). V_(H) polymorphism can be described in two principle forms. The first is variation arising from allelic variation associated with differences among the nucleotide sequence between alleles of the same gene segment. The second arises from the numerous duplications, insertions, and/or deletions that have occurred at the immunoglobulin heavy chain locus. This has resulted in the unique situation in which V_(H) genes derived by duplication from identical genes differ from their respective alleles by one or more nucleotide substitutions. This also directly influences the copy number of V_(H) genes at the heavy chain locus.

Polymorphic alleles of the human immunoglobulin heavy chain variable gene segments (V_(H) genes) have largely been the result of insertion/deletion of gene segments and single nucleotide differences within coding regions, both of which have the potential to have functional consequences on the immunoglobulin molecule. Table 1 sets forth the functional V_(H) genes listed by human V_(H) gene family and the number of identified alleles for each V_(H) gene in the human immunoglobulin heavy chain locus. There are some findings to suggest that polymorphic V_(H) genes have been implicated in susceptibility to certain diseases such as, for example, rheumatoid arthritis, whereas in other cases a linkage between V_(H) and disease has been less clear. This ambiguity has been attributed to the copy number and presence of various alleles in different human populations. In fact, several human V_(H) genes demonstrate copy number variation (e.g., V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, and V_(H)3-23). In various embodiments, humanized mice as described herein with restricted V_(H) repertoires comprise multiple polymorphic variants of an individual V_(H) family member (e.g., two or more polymorphic variants of V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, or V_(H)3-23, replacing all or substantially all functional mouse V_(H) segments at an endogenous mouse locus). In a specific embodiment, the two or more polymorphic variants of mice described herein are in number up to and including the number indicated for the corresponding V_(H) family member in Table 1 (e.g., for V_(H)1-69, 13 variants; for V_(H)1-2, five variants; etc.).

Commonly observed variants of particular human V_(H) genes are known in the art. For example, one of the most complex polymorphisms in the V_(H) locus belongs to the V_(H)1-69 gene. The human V_(H)1-69 gene has 13 reported alleles (Sasso et al., 1993, A fetally expressed immunoglobulin V_(H)1 gene belongs to a complex set of alleles, Journal of Clinical Investigation 91:2358-2367; Sasso et al., 1996, Expression of the immunoglobulin V_(H) gene 51p1 is proportional to its germline gene copy number, Journal of Clinical Investigation 97 (9):2074-2080) and exists in at least three haplotypes that carry duplications of the V_(H)1-69 gene, which results in multiple copies of the V_(H) gene at a given locus. These polymorphic alleles include differences in the complementarity determining regions (CDRs), which may dramatically influence antigen specificity. Table 2 sets for the reported alleles for human V_(H)1-69 and the SEQ ID NOs for the DNA and protein sequences of the mature heavy chain variable regions. Table 3 sets forth the reported alleles for human V_(H)1-2 genes and the SEQ ID NOs for the DNA and protein sequences of the mature heavy chain variable regions. 240

Representative genomic DNA and full-length protein sequences of a V_(H)1-69 gene are set forth in SEQ ID NO: 1 and SEQ ID NO: 2, respectively. FIG. 13 and FIG. 14 set forth DNA and protein alignments of thirteen reported V_(H)1-69 alleles, respectively. Representative DNA and protein sequences of a V_(H)1-2 gene are set forth in SEQ ID NO: 60 and SEQ ID NO: 61, respectively. FIG. 16 and FIG. 17 set forth DNA and protein alignments of five reported V_(H)1-2 alleles, respectively. FIG. 15 and FIG. 18 set forth a percent identity/similarity matrix for aligned protein sequences corresponding to thirteen reported human V_(H)1-69 alleles and five reported human V_(H)1-2 alleles, respectively. In various embodiments, the modified locus of the invention comprises a V_(H) gene selected from Table 1, present in two or more copy number, wherein the copy number includes up to and including the number of alleles shown in Table 1. In one embodiment, the modified locus of the invention comprises a V_(H)1-69 gene selected from Table 2, present in two or more copy number, wherein the copy number includes up to and including the number of alleles shown in Table 1. In one embodiment, the modified locus of the invention comprises a V_(H)1-2 gene selected from Table 3, present in two or more copy number, wherein the copy number includes up to and including the number of alleles shown in Table 1.

Although embodiments employing a restricted human V_(H) repertoire in a mouse are extensively discussed, other non-human animals that express a restricted human V_(H) repertoire are also provided. Such non-human animals include any of those which can be genetically modified to express a restricted human V_(H) repertoire as disclosed herein, including, e.g., mouse, rat, rabbit, pig, bovine (e.g., cow, bull, buffalo), deer, sheep, goat, chicken, cat, dog, ferret, primate (e.g., marmoset, rhesus monkey), etc. For example, for those non-human animals for which suitable genetically modifiable ES cells are not readily available, other methods are employed to make a non-human animal comprising the genetic modification. Such methods include, e.g., modifying a non-ES cell genome (e.g., a fibroblast or an induced pluripotent cell) and employing nuclear transfer to transfer the modified genome to a suitable cell, e.g., an oocyte, and gestating the modified cell (e.g., the modified oocyte) in a non-human animal under suitable conditions to form an embryo. Methods for modifying a non-human animal genome (e.g., a pig, cow, rodent, chicken, etc. genome) include, e.g., employing a zinc finger nuclease (ZFN) or a transcription activator-like effector nuclease (TALEN) to modify a genome to include a restricted human V_(H) repertoire. Thus, in one embodiment a method is provided for editing a non-human animal genome to include a restricted human V_(H) repertoire, comprising a step of editing the genome employing a ZFN or a TALEN to include no more than one, or no more than two, human V_(H) gene segments (or polymorphic variants thereof), wherein the no more than one or no more than two human V_(H) gene segments are operably linked to an immunoglobulin constant gene sequence. In one embodiment, the constant gene sequence is selected from a human heavy chain constant sequence and a non-human heavy chain constant sequence. In one embodiment, the constant sequence is non-human and the no more than one or no more than two human V_(H) gene segments are operably linked to non-human constant gene sequence at an endogenous non-human immunoglobulin locus.

In one aspect, the non-human animal is a small mammal, e.g., of the superfamily Dipodoidea or Muroidea. In one embodiment, the genetically modified animal is a rodent. In one embodiment, the rodent is selected from a mouse, a rat, and a hamster. In one embodiment, the rodent is selected from the superfamily Muroidea. In one embodiment, the genetically modified animal is from a family selected from Calomyscidae (e.g., mouse-like hamsters), Cricetidae (e.g., hamster, New World rats and mice, voles), Muridae (true mice and rats, gerbils, spiny mice, crested rats), Nesomyidae (climbing mice, rock mice, with-tailed rats, Malagasy rats and mice), Platacanthomyidae (e.g., spiny dormice), and Spalacidae (e.g., mole rates, bamboo rats, and zokors). In a specific embodiment, the genetically modified rodent is selected from a true mouse or rat (family Muridae), a gerbil, a spiny mouse, and a crested rat. In one embodiment, the genetically modified mouse is from a member of the family Muridae,

In one embodiment, the non-human animal is a rodent that is a mouse of a C57BL strain. In one embodiment, the C57BL strain is selected from C57BL/A, C57BL/An, C57BL/GrFa, C57BL/KaLwN, C57BL/6, C57BL/6J, C57BL/6ByJ, C57BL/6N, C57BL/6NJ, C57BL/10, C57BL/10ScSn, C57BL/10Cr, and C57BL/OIa. In another embodiment, the mouse is a 129 strain. In one embodiment, the 129 strain is selected from the group consisting of 129P1, 129P2, 129P3, 129X1, 129S1 (e.g., 129S1/SV, 129S1/SvIm), 129S2, 129S4, 129S5, 129S9/SvEvH, 129S6 (129/SvEvTac), 129S7, 129S8, 129T1, 129T2 (see, e.g., Festing et al. (1999) Revised nomenclature for strain 129 mice, Mammalian Genome 10:836, see also, Auerbach et al. (2000) Establishment and Chimera Analysis of 129/SvEv- and C57BL/6-Derived Mouse Embryonic Stem Cell Lines). In one embodiment, the genetically modified mouse is a mix of an aforementioned 129 strain and an aforementioned C57BL strain (e.g., a C57BL/6 strain). In another embodiment, the mouse is a mix of aforementioned 129 strains, or a mix of aforementioned C57BL/6 strains. In one embodiment, the 129 strain of the mix is a 129S6 (129/SvEvTac) strain. In another embodiment, the mouse is a mix of a 129/SvEv- and a C57BL/6-derived strain. In a specific embodiment, the mouse is a mix of a 129/SvEv- and a C57BL/6-derived strain as described in Auerbach et al. 2000 BioTechniques 29:1024-1032. In another embodiment, the mouse is a BALB strain, e.g., BALB/c strain. In another embodiment, the mouse is a mix of a BALB strain (e.g., BALB/c strain) and another aforementioned strain.

In one embodiment, the non-human animal is a rat. In one embodiment, the rat is selected from a Wistar rat, an LEA strain, a Sprague Dawley strain, a Fischer strain, F344, F6, and Dark Agouti. In one embodiment, the rat strain is a mix of two or more of a strain selected from the group consisting of Wistar, LEA, Sprague Dawley, Fischer, F344, F6, and Dark Agouti.

TABLE 1 V_(H) Family V_(H) Gene Alleles V_(H)1 1-2 5 1-3 2 1-8 2 1-18 3 1-24 1 1-45 3 1-46 3 1-58 2 1-69 13 V_(H)2 2-5 10 2-26 1 2-70 13 V_(H)3 3-7 3 3-9 2 3-11 4 3-13 4 3-15 8 3-16 2 3-20 1 3-21 4 3-23 5 3-30 19 3-30-3 2 3-30-5 1 3-33 6 3-35 1 3-38 2 3-43 2 3-48 4 3-49 5 3-53 4 3-64 5 3-66 4 3-72 2 3-73 2 3-74 3 V_(H)4 4-4 7 4-28 6 4-30-1 1 4-30-2 5 4-30-4 6 4-31 10 4-34 13 4-39 7 4-59 10 4-61 8 V_(H)5 5-51 5 V_(H)6 6-1 2 V_(H)7 7-4-1 5 7-81 1

TABLE 2 SEQ ID NO: IgHV1-69 Allele Accession Number (DNA/Protein) IgHV1-69*01 L22582 34/35 IgHV1-69*02 Z27506 36/37 IgHV1-69*03 X92340 38/39 IgHV1-69*04 M83132 40/41 IgHV1-69*05 X67905 42/43 IgHV1-69*06 L22583 44/45 IgHV1-69*07 Z29978 46/47 IgHV1-69*08 Z14309 48/49 IgHV1-69*09 Z14307 50/51 IgHV1-69*10 Z14300 52/53 IgHV1-69*11 Z14296 54/55 IgHV1-69*12 Z14301 56/57 IgHV1-69*13 Z14214 58/59

TABLE 3 SEQ ID NO: IgHV1-2 Allele Accession Number (DNA/Protein) IgHV1-2*01 X07448 60/61 IgHV1-2*02 X62106 62/63 IgHV1-2*03 X92208 64/65 IgHV1-2*04 Z12310 66/67 IgHV1-2*05 HM855674 68/69

Antigen-Dependent V_(H) Gene Usage

Antigen-dependent preferential usage of V_(H) genes can be exploited in the development of human therapeutics targeting clinically significant antigens. The ability to generate a repertoire of antibody variable domains using a particular V_(H) gene can provide a significant advantage in the search for high-affinity antibody variable domains to use in human therapeutics. Studies on naive mouse and human V_(H) gene usage in antibody variable domains reveal that most heavy chain variable domains are not derived from any particular single or dominantly used V_(H) gene. On the other hand, studies of antibody response to certain antigens reveal that in some cases a particular antibody response displays a biased usage of a particular V_(H) gene in the B cell repertoire following immunization.

Although the human V_(H) repertoire is quite diverse, by some estimates the expected frequency of usage of any given V_(H) gene, assuming random selection of V_(H) genes, is about 2% (Brezinschek et al., 1995, Analysis of the Heavy Chain Repertoire of Human Peripheral B Cells Using Single-Cell Polymerase Chain Reaction, J. Immunol. 155:190-202). But V_(H) usage in peripheral B cells in humans is skewed. In one study, functional V gene abundance followed the pattern V_(H)3>V_(H)4>V_(H)1>V_(H)2>V_(H)5>V_(H)6 (Davidkova et al., 1997, Selective Usage of V_(H) Genes in Adult Human Lymphocyte Repertoires, Scand. J. Immunol. 45:62-73). One early study estimated that V_(H)3 family usage frequency was about 0.65, whereas V_(H)1 family usage frequency was about 0.15; these and other observations suggest that the germline complexity of the human V_(H) repertoire is not precisely reflected in the peripheral B cell compartment in humans that have a normal germline V_(H) repertoire, a situation that is similar to that observed in the mouse—i.e., V_(H) gene expression is non-stochastic (Zouali and These, 1991, Probing V_(H) Gene-Family Utilization in Human Peripheral B Cells by In Situ Hybridization, J. Immunol. 146 (8):2855-2864). According to one report, V_(H) gene usage in humans, from greatest to least, is V_(H)3>V_(H)4>V_(H)1>V_(H)5>V_(H)2>V_(H)6; rearrangements in peripheral B cells reveal that V_(H)3 family usage is higher than to be expected based on the relative number of germline V_(H)3 genes (Brezinschek et al., 1995). According to another report V_(H) usage in humans follows the pattern V_(H)3>V_(H)5>V_(H)2>V_(H)1>V_(H)4>V_(H)6, based on analysis of pokeweed mitogen-activated peripheral small immunocompetent B cells (Davidkova et al., 1997, Selective Usage of V_(H) Genes in Adult Human B Lymphocyte Repertoires, Scand. J. Immunol. 45:62-73). One report asserts that among the most frequently used V_(H)3 family members are 3-23, 3-30 and 3-54 (Brezinschek et al., 1995). In the V_(H)4 family, member 4-59 and 4-4b were found relatively more frequently (Id.), as well as 4-39 and 4-34 (Brezinscheck et al., 1997, Analysis of the Human V_(H) Gene Repertoire, J. Clin. Invest. 99 (10):2488-2501). Others postulate that the activated heavy chain repertoire is skewed in favor of high V_(H)5 expression and lower V_(H)3 expression (Van Dijk-Hard and Lundkvist, 2002, Long-term kinetics of adult human antibody repertoires, Immunology 107:136-144). Other studies assert that the most commonly used V_(H) gene in the adult human repertoire is V_(H)4-59, followed by V_(H)3-23 and V_(H)3-48 (Arnaout et al., 2001, High-Resolution Description of Antibody Heavy-Chain Repertoires in Humans, PLoS ONE 6 (8):108). Although usage studies are based on relatively small sample numbers and thus exhibit high variance, taken together the studies suggest that V gene expression is not purely stochastic. Indeed, studies with particular antigens have established that—in certain cases—the deck is firmly stacked against certain usages and in favor of others.

Over time, it became apparent that the observed repertoire of human heavy chain variable domains generated in response to certain antigens is highly restricted. Some antigens are associated almost exclusively with neutralizing antibodies having only certain particular V_(H) genes, in the sense that effective neutralizing antibodies are derived from essentially only one V_(H) gene. Such is the case for a number of clinically important human pathogens.

V_(H)1-69-derived heavy chains have been observed in a variety of antigen-specific antibody repertoires of therapeutic significance. For instance, V_(H)1-69 was frequently observed in heavy chain transcripts of an IgE repertoire of peripheral blood lymphocytes in young children with atopic disease (Bando et al., 2004, Characterization of V_(H)ε gene expressed in PBL from children with atopic diseases: detection of homologous V_(H)1-69 derived transcripts from three unrelated patients, Immunology Letters 94:99-106). V_(H)1-69-derived heavy chains with a high degree of somatic hypermutation also occur in B cell lymphomas (Perez et al., 2009, Primary cutaneous B-cell lymphoma is associated with somatically hypermutated immunoglobulin variable genes and frequent use of V_(H)1-69 and V_(H)4-59 segments, British Journal of Dermatology 162:611-618), whereas some V_(H)1-69-derived heavy chains with essentially germline sequences (i.e., little to no somatic hypermutation) have been observed among autoantibodies in patients with blood disorders (Pos et al., 2008, V_(H)1-69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura, Journal of Thrombosis and Haemostasis 7:421-428).

Further, neutralizing antibodies against viral antigens such as HIV, influenza and hepatitis C (HCV) have been found to utilize germline and/or somatically mutated V_(H)1-69-derived sequences (Miklos et al., 2000, Salivary gland mucosa-associated lymphoid tissue lymphoma immunoglobulin V_(H) genes show frequent use of V1-69 with distinctive CDR3 features, Blood 95 (12):3878-3884; Kunert et al., 2004, Characterization of molecular features, antigen-binding, and in vitro properties of IgG and IgM variants of 4E10, an anti-HIV type I neutralizing monoclonal antibody, Aids Research and Human Retroviruses 20 (7):755-762; Chan et al., 2001, V_(H)1-69 gene is preferentially used by hepatitis C virus-associated B cell lymphomas and by normal B cells responding to the E2 viral antigen, Blood 97 (4):1023-1026; Carbonari et al., 2005, Hepatitis C virus drives the unconstrained monoclonal expansion of V_(H)1-69-expressing memory B cells in type II cryoglobulinemia: A model of infection-driven lymphomagenesis, Journal of Immunology 174:6532-6539; Wang and Palese, 2009, Universal epitopes of influenza virus hemagglutinins?, Nature Structural & Molecular Biology 16 (3):233-234; Sui et al., 2009, Structural and functional bases for broad-spectrum neutralization of avian and human influenza A viruses, Nature Structural & Molecular Biology 16 (3):265-273; Marasca et al., 2001, Immunoglobulin Gene Mutations and Frequent Use of V_(H)1-69 and V_(H)4-34 Segments in Hepatitis C Virus-Positive and Hepatitis C Virus-Negative Nodal Marginal Zone B-Cell Lymphoma, Am. J. Pathol. 159 (1):253-261).

V_(H) usage bias is also observed in the humoral immune response to Haemophilus influenzae type b (Hib PS) in humans. Studies suggest that the V_(H)III family (the V_(H)IIIb subfamily in particular, V_(H)9.1) exclusively characterizes the human humoral response to Hib PS, with diverse D and J genes (Adderson et al., 1991, Restricted Ig H Chain V Gene Usage in the Human Antibody Response to Haemophilus influenzae Type b Capsular Polysaccharide, J. Immunol. 147 (5):1667-1674; Adderson et al., 1993, Restricted Immunoglobulin V_(H) Usage and VDJ Combinations in the Human Response to Haemophilus influenzae Type b Capsular Polysaccharide, J. Clin. Invest. 91:2734-2743). Human J_(H) genes also display biased usage; J_(H)4 and J_(H)6 are observed at about 38-41% in peripheral B cells in humans (Brezinschek et al., 1995).

V_(H) usage in HIV-1-infected humans is reportedly biased against V_(H)3 usage and in favor of V_(H)1 and V_(H)4 gene families (Wisnewski et al., 1996, Human Antibody Variable Region Gene Usage in HIV-1 Infection, J. Acquired Immune Deficiency Syndromes & Human Retroviology 11 (1):31-38). However, cDNA analysis of bone marrow from affected patients' revealed significant V_(H)3 usage not expressed in the functional B cell repertoire, where Fabs reflecting the V_(H)3 usage exhibited effective in vitro neutralization of HIV-1 (Id.). It might be postulated that the humoral immune response to HIV-1 infection is possibly attenuated due to the V_(H) restriction; modified non-human animals as described herein (not infectable by HIV-1) might thus be useful for generating neutralizing antibody domains derived from particular V_(H) genes present in the genetically modified animals described herein, but derived from different V_(H) genes than those observed in the restricted repertoire of affected humans.

Thus, the ability to generate high affinity human antibody variable domains in V_(H)-restricted mice, e.g., (restricted, e.g., to a V_(H)3 family member and polymorph(s) thereof) immunized with HIV-1 might provide a rich resource for designing effective HIV-1-neutralizing human therapeutics by thoroughly mining the restricted (e.g., restricted to a V_(H)3 family member or variant(s) thereof) repertoire of such an immunized mouse.

Restriction of the human antibody response to certain pathogens may reduce the likelihood of obtaining antibody variable regions from affected humans that can serve as springboards for designing high affinity neutralizing antibodies against the pathogen. For example, the human immune response to HIV-1 infection is clonally restricted throughout HIV-1 infection and into AIDS progression (Muller et al., 1993, B-cell abnormalities in AIDS: stable and clonally restricted antibody response in HIV-1 infection, Scand. J. Immunol. 38:327-334; Wisnewski et al., 1996). Further, V_(H) genes are in general not present in all polymorphic forms in any particular individual; certain individuals in certain populations possess one variant, whereas individuals in other populations possess a different variant. Thus, the availability of a biological system that is restricted to a single V_(H) gene and its variants will in various embodiments provide a hitherto unexploited source of diversity for generating antibody variable regions (e.g., human heavy and light cognate domains) based on a restricted V_(H) gene. Thus, in one aspect, a genetically modified non-human animal is provided that comprises a plurality of polymorphic variants of no more than one, or no more than two, human V_(H) gene segment family member. In one embodiment, the no more than one, or no more than two, human V_(H) gene segments are operably linked to one or more human D_(H) gene segments, one or more human J_(H) gene segments, and a human or non-human constant region gene segment. In one embodiment the constant region is at an endogenous non-human immunoglobulin constant gene locus. In one embodiment, the non-human animal further comprises a nucleic acid sequence derived from a human V_(L) sequence, e.g., a rearranged or unrearranged human V_(L) gene segment or a rearranged human V_(L)/J_(L) sequence. In one embodiment, the nucleic acid sequence derived from the human V_(L) sequence is at an endogenous non-human V_(L) gene locus; in one embodiment, the nucleic acid sequence derived form the human V_(L) sequence is on a transgene. In a specific embodiment, the non-human animal is incapable of expressing an immunoglobulin light chain variable domain that itself comprises an endogenous V_(L) or J_(L) gene segment, and comprises no more than one, or no more than two, light chain genes that encode rearranged human V_(L) domains (Le., from no more than one, or no more than two, rearranged human V_(L)/J_(L) sequences).

Genetically modified mice that express human heavy chain variable regions with restricted V_(H) gene segment usage are useful to generate a relatively large repertoire of junctionally diverse, combinatorially diverse, and somatically mutated high affinity human immunoglobulin heavy chain variable regions from an otherwise restricted repertoire. A restricted repertoire, in one embodiment, refers to a predetermined limitation in the number and/or identity of germline genes that results in the mouse being unable to form a rearranged heavy chain gene that is derived from any V gene other than a preselected V gene. In embodiments that employ a preselected V gene but not a preselected D and/or J gene, the repertoire is restricted with respect to the identity of the V gene but not the D and/or J gene (e.g., the repertoire consists essentially of no more than one, or no more than two, V_(H) gene segments (and/or polymorphs thereof); and a plurality of D gene segments and a plurality of J gene segments)). The identity of the preselected V gene (and any preselected D and/or J genes) is not limited to any particular V gene.

Designing a mouse so that it rearranges a single V_(H) gene (present as a single segment or a set of variants) with a variety of human D and J gene segments (e.g., D_(H) and J_(H) segments) provides an in vivo junctional diversity/combinatorial diversity/somatic hypermutation permutation machine that can be used to iterate mutations in resulting rearranged heavy chain variable region sequences (e.g., V/D/J or V/J, as the case may be). In such a mouse, the clonal selection process operates to select suitable variable regions that bind an antigen of interest that are based on a single preselected V_(H) gene (or variants thereof). Because the mouse's clonal selection components are dedicated to selection based on the single preselected V_(H) gene segment, background noise (e.g., a wide variety of non antigen-binding V_(H) domains derived from many germline gene segments) is largely eradicated. With judicious selection of the V_(H) gene segment, a relatively larger number of clonally selected, antigen-specific antibodies can be screened in a shorter period of time than with a mouse with a large diversity of V segments.

Preselecting limited repertoire and restricting a mouse to a single V segment provides a system for permuting V/D/J junctions at a rate that is in various embodiments higher than that observed in mice that otherwise have up to 40 or more V segments to recombine with D and J regions. Removal of other V segments frees the locus to form more V/D/J combinations for the preselected V segment than otherwise observed. The increased number of transcripts that result from the recombination of the preselected V with one of a plurality of D and one of a plurality of J segments will feed those transcripts into the clonal selection system in the form of pre-B cells, and the clonal selection system is thus dedicated to cycling B cells that express the preselected V region. In this way, more unique V region rearrangements derived from the preselected V segment can be screened by the organism than would otherwise be possible in a given amount of time.

In various aspects, mice are described that enhance the junctional diversity of V/D/J recombinations for the preselected V region, because all or substantially all recombinations of the immunoglobulin heavy chain variable locus will be of the preselected V segment and the D and J segments that are placed in such mice. Therefore, the mice provide a method for generating a diversity of CDR3 segments using a base, or restricted V_(H) gene repertoire.

In one aspect, a non-human animal is provided, wherein the B cell population of the non-human animal expresses immunoglobulin heavy chains that are derived from no more than one, or no more than two human V_(H) gene segments. In one embodiment, each of the no more than one, or no more than two, human V_(H) gene segments are present in two or more polymorphic forms. In one embodiment, the human V_(H) gene segment is present in three, four, five, six, seven, eight, nine, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 polymorphic forms. In one embodiment, the non-human animal expresses a human light chain variable domain derived from a human V_(L) gene segment.

In one aspect, a method is provided for generating a B cell population in a non-human animal, wherein the B cell population expresses human heavy chains derived from a single germline human V_(H) gene segment and two or more human D gene segments and two or more human J gene segments; the method comprising a step of immunizing a non-human animal as described herein with an antigen of interest, and allowing the non-human animal to mount an immune response to the antigen of interest, wherein the immune response comprises expressing the human heavy chains on the surface of B cells in the B cell population In one embodiment, the non-human animal is a rodent (e.g., a mouse or rat). In one embodiment, the human V_(H) gene segment, human D_(H) segment, and human J_(H) segment are operably linked to a non-human constant region gene. In one embodiment, the non-human animal further comprises a nucleic acid sequence encoding a human V_(L) domain. In one embodiment, the nucleic acid sequence encoding the human V_(L) domain is linked to a non-human light chain constant region gene sequence.

In one aspect, a method for making a non-human animal that expresses an immunoglobulin population characterized by the immunoglobulins having heavy chains that are derived from a plurality of rearrangements of a single human V_(H) gene segment (or sing human V_(H) gene family member) and one of a plurality of D_(H) gene segments and one of a plurality of J_(H) gene segments, is provided. In one embodiment, the human V_(H) gene segment is a human V_(H)1-69 gene segment. In one embodiment, the human V_(H) gene segment is a human V_(H)1-2 gene segment.

In one aspect, a method is provided for generating a population of human immunoglobulin heavy chain variable domains whose CDR1 and CDR2 are derived from the same germline V_(H) gene segment, and whose CDR3 are derived from the germline gene segment and two or more human D segments, and two or more human J segments; the method comprising immunizing a non-human animal as described herein with an antigen of interest, and allowing the non-human animal to mount an immune response to the antigen of interest, wherein the immune response comprises expressing the human heavy chain variable domains in the context of a light chain variable domain. In one embodiment, the non-human animal is a rodent (e.g., a mouse or rat). In one embodiment, the human V_(H) gene segment, human D segment, and human J segment are operably linked to a non-human constant region gene. In one embodiment, the non-human animal further comprises a nucleic acid sequence encoding a human V_(L) domain. In one embodiment, the nucleic acid sequence encoding the human V_(L) domain is linked to a non-human light chain constant region gene sequence.

In one aspect, a genetically modified non-human animal is provided, wherein the non-human animal is incapable of expressing a non-human V_(H) domain, and wherein each immunoglobulin heavy chain of the heavy chain population expressed in the animal comprises a human V_(H) domain comprising a CDR1 and a CDR2 that are identical but for one or more somatic hypermutations, and wherein the heavy chain population comprises a plurality of CDR3 sequences derived from a plurality of rearrangements with a plurality of D and J gene segments.

In one aspect, a biological system for generating variation in CDR3 identity and length is provided, comprising a genetically modified non-human animal as described herein, wherein the non-human animal comprises no more than or no more than two human V_(H) gene segments, and two or more D gene segments and one or more J gene segments, wherein the non-human animal further comprises a humanized immunoglobulin light chain locus. In various embodiments, the non-human animal in response to immunization with an antigen of interest generates an immune response that comprises expressing an immunoglobulin heavy chain population characterized by each heavy chain having CDR1s and CDR2s that differ only by somatic hypermutation, and CDR3s that differ by rearrangement and somatic hypermutation. In one embodiment, the biological system is a mouse that is genetically modified as described herein. In one embodiment, the human V_(H) gene segment and the human V_(L) gene segment are at endogenous mouse heavy and light immunoglobulin loci, respectively. In one embodiment, one or more of the human V_(H) gene segment and the human V_(L) gene segment are on transgenes (i.e., at a locus other than an endogenous immunoglobulin locus).

EXAMPLES

The following examples are provided so as to describe to those of ordinary skill in the art how to make and use methods and compositions of the invention, and are not intended to limit the scope of what the inventors regard as their invention. Unless indicated otherwise, temperature is indicated in Celsius, and pressure is at or near atmospheric. In the foregoing Examples, when the use of kits and/reagents from various suppliers is indicated, all procedures were carried out according to manufacturer's specifications.

Example 1 Construction of Restricted Heavy Chain Loci

A uniquely engineered human heavy chain locus containing a single human V_(H) gene segment located upstream of all the human D_(H) and J_(H) gene segments was created by a series of homologous recombination reactions in bacterial cells (BHR) using Bacterial Artificial Chromosome (BAC) DNA. Several targeting constructs for creation of a single V_(H) containing heavy chain locus were constructed using VELOCIGENE® genetic engineering technology (see, e.g., U.S. Pat. No. 6,586,251 and Valenzuela, D. M. et al. (2003) High-throughput engineering of the mouse genome coupled with high-resolution expression analysis. Nature Biotechnology 21 (6): 652-659).

Construction of a Human V_(H)1-69 Restricted Heavy Chain Locus. Briefly, four modifications were performed using human BAC DNA to create a targeting construct containing a human V_(H)1-69 gene segment with all the human D_(H) and J_(H) segments (FIG. 1). In the first modification, a modified human BAC containing multiple distal (5′) human V_(H) gene segments, including V_(H)1-69, an upstream hygromycin selection cassette and a 5′ mouse homology arm was targeted with a second spectinomycin cassette, which also contained a modified recombination signal sequence (RSS; BHR 1, FIG. 1, top left). This modified recombination signal sequence (RSS) introduced two point mutations (T to A and G to A) in the 3′ RSS region of the human V_(H)1-69 gene changing the RSS nonamer to the optimal consensus sequence. Thus, the first modification (BHR 1) created a human genomic fragment containing the human V_(H)1-69 gene segment with a modified 3′ RSS, a unique AsiSI restriction site about 180 bp downstream of the RSS and a spectinomycin cassette (FIG. 1, middle left).

The second modification (BHR 2) included the use of a neomycin (Neo) cassette flanked by Frt sites to delete the hygromycin cassette and 5′ human V_(H) gene segments upstream of the V_(H)1-69 gene segment. This modification was targeted 5′ to the human V_(H)1-69 gene segment to leave intact about 8.2 kb of the promoter region of human V_(H)1-69 and the 5′ mouse homology arm (FIG. 1, bottom left).

The third modification (BHR 3) included another spectinomycin cassette flanked by uniquely engineered 5′ PI-SceI and 3′ AsiSI sites targeted to a human genomic fragment containing the first three functional human V_(H) gene segments and all the human D_(H) and J_(H) gene segments (FIG. 1, middle right). The human genomic fragment was previously targeted with a neomycin cassette and contained 5′ and 3′ homology arms containing the mouse genomic sequence 5′ and 3′ of the endogenous heavy chain locus including the 3′ intronic enhancer and the IgM gene. This modification deleted the 5′ mouse genomic sequence and human V_(H) gene segments, leaving about 3.3 kb of the V_(H)-D_(H) intergenic region upstream of the human D_(H)1-1 gene segment, all of the human D_(H) and J_(H) segments, and the 3′ mouse genomic fragment containing the 3′ intronic enhancer and the IgM gene (FIG. 1, bottom right).

The fourth modification was achieved by employing the unique PI-SceI and AsiSI sites (described above) to ligate the two modified BACs from BHR 2 and BHR 3 (FIG. 1, bottom center), which yielded the final targeting construct. The final targeting construct for the creation of a modified heavy chain locus containing a single human V_(H) gene segment and all the human D_(H) and J_(H) gene segments in ES cells contained, from 5′ to 3′, a 5′ homology arm containing about 20 kb of mouse genomic sequence upstream of the endogenous heavy chain locus, a 5′ Frt site, a neomycin cassette, a 3′ Frt site, about 8.2 kb of the human V_(H)1-69 promoter, the human V_(H)1-69 gene segment with a modified 3′ RSS, 27 human D_(H) gene segments, six human J_(H) segments, and a 3′ homology arm containing about 8 kb of mouse genomic sequence downstream of the mouse J_(H) gene segments including the 3′ intronic enhancer and IgM gene (FIG. 1, bottom). The Human V_(H)1-69 Targeting Vector (SEQ ID NO: 3) was linearized and electroporated into mouse ES cells heterozygous for a deletion of the endogenous heavy chain locus.

Construction of a Human V_(H)1-2 Restricted Heavy Chain Locus. Using the steps described above, other polymorphic V_(H) gene segments in the context of mouse heavy chain constant regions are employed to construct a series of mice having a restricted number immunoglobulin heavy chain V segments (e.g., 1, 2, 3, 4, or 5), wherein the V segments are polymorphic variants of a V gene family member. Exemplary polymorphic V_(H) gene segments are derived from human V_(H) gene segments including, e.g., V_(H)1-2, V_(H)2-26, V_(H)2-70 and V_(H)3-23. Such human V_(H) gene segments are obtained, e.g., by de novo synthesis (e.g., Blue Heron Biotechnology, Bothell, Wash.) using sequences available on published databases. Thus, DNA fragments encoding each V_(H) gene are, in some embodiments, generated independently for incorporation into targeting vectors, as described herein. In this way, multiple modified immunoglobulin heavy chain loci comprising a restricted number of V_(H) gene segments are engineered in the context of mouse heavy chain constant regions. An exemplary targeting strategy for creating a restricted humanized heavy chain locus containing a human V_(H)1-2 gene segment, 27 human D_(H) gene segments, and six human J_(H) gene segments is shown in FIG. 2.

Briefly, a modified human BAC clone containing three human V_(H) gene segments (V_(H)6-1, V_(H)1-2, V_(H)1-3), 27 human D_(H) gene segments, and six human J_(H) gene segments (see U.S. Ser. No. 13/404,075; filed 24 Feb. 2012, herein incorporated by reference) is used to create a restricted humanized heavy chain locus containing a human V_(H)1-2 gene segment. This modified BAC clone functionally links the aforementioned human heavy chain gene segments with the mouse intronic enhancer and the IgM constant region. The restricted human V_(H)1-2 based heavy chain locus is achieved by two homologous recombinations using the modified human BAC clone described above.

For the first homologous recombination, 205 bp of the human V_(H)6-1 gene segment (from about 10 bp upstream (5′) of the V_(H)6-1 start codon in exon 1 to about 63 bp downstream (3′) of the beginning of exon 2) in the modified human BAC clone is deleted by bacterial homologous recombination using a spectinomycin (aadA) cassette flanked by unique PI-SceI restriction sites (FIG. 2, BHR 1). This allows for subsequent removal of the aadA cassette without disrupting other human gene segments within the restricted heavy chain locus.

For the second homologous recombination, the 5′ end of the modified human BAC clone including the entire human V_(H)1-3 gene segment and about 60 bp downstream (3′) of the gene segment is deleted by homologous recombination using a hygromycin cassette containing flanking 5′ AsiSI and 3′ AscI restriction sites (FIG. 2, BHR 2). As described above, the spectinomycin cassette is optionally removed after confirmation of the final targeting vector including deletion of the two human V_(H) gene segments flanking the human V_(H)1-2 gene segment (FIG. 2, bottom). An exemplary human V_(H)1-2 targeting vector is set forth in SEQ ID NO: 70.

Employing polymorphic V_(H) gene segments in a restricted immunoglobulin heavy chain locus represents a novel approach for generating antibodies, populations of antibodies, and populations of B cells that express antibodies having heavy chains with diverse CDRs derived from a single human V_(H) gene segment. Exploiting the somatic hypermutation machinery of the host animal along with combinatorial association with rearranged human immunoglobulin light chain variable domains results in the engineering of unique heavy chains and unique V_(H)/V_(L) pairs that expand the immune repertoire of genetically modified animals and enhance their usefulness as a next generation platform for making human therapeutics, especially useful as a platform for making neutralizing antibodies specific for human pathogens.

Thus, using the strategy outlined above for incorporation of additional and/or other polymorphic V_(H) gene segments into the mouse immunoglobulin heavy chain locus allows for the generation of novel antibody repertoires for use in neutralizing human pathogens that might otherwise effectively evade the host immune system.

Targeted ES cells described above were used as donor ES cells and introduced into an 8-cell stage mouse embryo by the VELOCIMOUSE® method (supra). Mice bearing a humanized heavy chain locus containing a single human V_(H) gene segment, all the human D_(H) and J_(H) gene segments operably linked to the mouse immunoglobulin constant region genes were identified by genotyping using a modification of allele assay (Valenzuela et al., supra) that detected the presence of the neomycin cassette, the human V_(H) gene segment and a region within the human D_(H) and J_(H) gene segments as well as endogenous heavy chain sequences. Table 4 sets forth the primers and probes used in this assay to confirm mice harboring a restricted heavy chain locus containing a single human V_(H)1-69 gene segment, 27 human D_(H) gene segments and six human J_(H) gene segments.

Mice bearing an engineered heavy chain locus that contains a single human V_(H) gene segment can be bred to a FLPe deletor mouse strain (see, e.g., Rodriguez, C. I. et al. (2000) High-efficiency deleter mice show that FLPe is an alternative to Cre-IoxP. Nature Genetics 25: 139-140) in order to remove any Frt'ed neomycin cassette introduced by the targeting vector that is not removed, e.g., at the ES cell stage or in the embryo. Optionally, the neomycin cassette is retained in the mice.

Pups are genotyped and a pup heterozygous for a humanized heavy chain locus containing a single human V_(H) gene segment, all the human D_(H) and J_(H) segments operably linked to the endogenous mouse immunoglobulin constant genes is selected for characterizing the immunoglobulin heavy chain repertoire.

TABLE 4 Name SEQ ID (Region Detected) Sequence (5′-3′) NO: hyg Forward: TGCGGCCGAT CTTAGCC 4 (hygromycin Reverse: TTGACCGATT CCTTGCGG 5 cassette) Probe: ACGAGCGGGT TCGGCCCATT C 6 neo Forward: GGTGGAGAGG CTATTCGGC 7 (neomycin Reverse: GAACACGGCG GCATCAG 8 cassette) Probe: TGGGCACAAC AGACAATCGG CTG 9 hIgH9T Forward: TCCTCCAACG ACAGGTCCC 10 (human D_(H)-J_(H) Reverse: GATGAACTGA CGGGCACAGG 11 genomic Probe: TCCCTGGAAC TCTGCCCCGA CACA 12 sequence) 77h3 Forward: CTCTGTGGAA AATGGTATGG AGATT 13 (human V_(H)1-69 Reverse: GGTAAGCATA GAAGGTGGGT ATCTTT 14 gene segment) Probe: ATAGAACTGT CATTTGGTCC AGCAATCCCA 15 mIgHA7 Forward: TGGTCACCTC CAGGAGCCTC 16 (mouse D_(H)-J_(H) Reverse: GCTGCAGGGT GTATCAGGTG C 17 genomic Probe: AGTCTCTGCT TCCCCCTTGT 18 sequence) GGCTATGAGC 88710T Forward: GATGGGAAGA GACTGGTAAC ATTTGTAC 19 (mouse 3′ V_(H) Reverse: TTCCTCTATT TCACTCTTTG AGGCTC 20 genomic Probe: CCTCCACTGT GTTAATGGCT GCCACAA 21 sequence) mIgHd10 Forward: GGTGTGCGAT GTACCCTCTG AAC 22 (mouse 5′ V_(H) Reverse: TGTGGCAGTT TAATCCAGCT TTATC 23 genomic Probe: CTAAAAATGC TACACCTGGG 24 sequence) GCAAAACACC TG mIgHp2 Forward: GCCATGCAAG GCCAAGC 25 (mouse J_(H) Reverse: AGTTCTTGAG CCTTAGGGTG CTAG 26 genomic Probe: CCAGGAAAAT GCTGCCAGAG CCTG 27 sequence)

Example 2 Characterization of Mice Expressing Heavy Chains Derived From a Single Human V_(H) Gene Segment

Mice homozygous for a single human V_(H) gene segment at the endogenous heavy chain locus as described in Example 1 were evaluated for expression and B cell development using flow cytometry.

Briefly, spleens and bone marrow was harvested from wild type (n=3 per group; six weeks old, male and female) and mice homozygous for a single human V_(H) gene segment, all human D_(H) and J_(H) gene segments operably linked to mouse heavy chain constant regions. Red blood cells from spleens were lysed with ACK lysis buffer (Lonza Walkersville), followed by washing with complete RPMI medium.

Flow cytometry. Cells (1×10⁶) were incubated with anti-mouse CD16/CD32 (2.4G2, BD PHARMINGEN™) on ice for 10 minutes, followed by labeling with the following antibody panels for 30 minutes on ice. Bone marrow panel: anti-mouse FITC-CD43 (1B11, BioLegend), PE-ckit (2B8, BIOLEGEND®), PeCy7-IgM (II/41, EBIOSCIENCE®), PerCP-Cy5.5-IgD (11-26c.2a, BIOLEGEND®), APC-eFluor 780-6220 (RA3-6B2, EBIOSCIENCE®), APC-CD19 (MB19-1, EBIOSCIENCE®). Bone marrow and spleen panel: anti-mouse FITC-Igκ (187.1, BD Biosciences), PE-Igλ (RML-42, BIOLEGEND®), PeCy7-IgM (II/41, EBIOSCIENCE®), PerCP-Cy5.5-IgD (11-26c.2a, BIOLEGEND®), Pacific Blue-CD3 (17A2, BIOLEGEND®), APC-B220 (RA3-6B2, EBIOSCIENCE®), APC-H7-CD19 (ID3, BD Biosciences). Bone marrow: immature B cells (B220^(int)IgM⁺), mature B cells (B220^(hi)IgM⁺), pro B cells (CD19⁺ckit⁺CD43⁺), pre B cells (CD19⁺ckit⁻CD43⁻), immature Igκ⁺ B cells (B220^(int)IgM⁺Igκ⁺Igλ⁻), immature Igλ⁺ B cells (B220^(int)IgM⁺Igκ⁻Igλ⁺), mature Igκ⁺ B cells (B220^(hi)IgM⁺Igκ⁺Igλ⁻), mature Igλ⁺ B cells (B220^(hi)IgM⁺Igκ⁻Igλ⁺). Spleen: B cells (CD19⁺), mature B cells (CD19⁺IgD^(hi)IgM^(int)), transitional/immature B cells (CD19⁺IgD^(int)IgM^(hi)). Bone marrow and spleen: Igκ⁺ B cells (CD19⁺Igκ⁺Igλ⁻), Igλ⁺ B cells (CD19⁺Igκ⁻Igλ⁺).

Following staining, cells were washed and fixed in 2% formaldehyde. Data acquisition was performed on a LSRII flow cytometer and analyzed with FLOWJO™ software (Tree Star, Inc.). Results for the splenic compartment are shown in FIGS. 3, 4A and 5-7. Results for the bone marrow compartment are shown in FIGS. 4B and 8-11B.

Human V_(H) Expression. Expression of the human V_(H)1-69 gene segment was determined for mice heterozygous and homozygous for a human V_(H)1-69 gene segment, all human D_(H) and J_(H) gene segments operably linked to mouse heavy chain constant regions by a quantitative PCR assay using TAQMAN® probes.

Briefly, CD19⁺ B cells were purified from the spleens of groups of mice (n=3 per group) using mouse CD19 microbeads (Miltenyi Biotec) according to manufacturer's specifications. Total RNA was purified using the RNEASY™ Mini kit (Qiagen) and genomic RNA was removed using an RNase-free DNase on-column treatment (Qiagen). About 200 ng mRNA was reverse-transcribed into cDNA using the First Stand cDNA Synthesis kit (Invitrogen), followed by amplification with the TAQMAN® Universal PCR Master Mix (Applied Biosystems) using the ABI 7900 Sequence Detection System (Applied Biosystems). Unique primer/probe combinations were employed to specifically determine expression of human V_(H)1-69-derived heavy chains (Table 5). Relative expression was normalized to the mouse κ constant region (mCκ). The results are shown in FIG. 12.

TABLE 5 Sequence SEQ ID Name (5′-3′) NO: hIgHV1-69 Sense: AACTACGCAC AGAAGTTCCA GG 28 Anti-sense: GCTCGTGGAT TTGTCCGC 29 Probe: CAGAGTCACG ATTACC 30 mCκ Sense: TGAGCAGCAC CCTCACGTT 31 Antisense: GTGGCCTCAC AGGTATAGCT 32 GTT Probe: ACCAAGGACG AGTATGAA 33

Example 3 Humoral Immune Response in Mice Expressing Heavy Chains Derived From a Single Human V_(H) Gene Segment

The humoral immune response was determined for mice homozygous for human heavy and κ light chain variable gene loci (H_(κ)) and mice homozygous for a single human V_(H) gene segment, all human D_(H) and J_(H) gene segments operably linked to mouse heavy chain constant regions (1hV_(H) HO) by comparative immunization using a human cell surface receptor (Antigen A).

Immunization. Serum was collected from groups of mice prior to immunization with the above antigen. Antigen (2.35 μg each) was administered in an initial priming immunization mixed with 10 μg of CpG oligonucleotide (Invivogen) and 25 μg of Adju-phos (Brenntag) as adjuvants. The immunogen was administered via footpad (f.p.) in a volume of 25 μl per mouse. Subsequently, mice were boosted via f.p. with 2.3 μg of antigen along with 10 μg CpG and 25 μg Adju-Phos as adjuvants on days 3, 6, 11, 13, 17, and 20 for a total of six boosts. Mice were bled on days 15 and 22 after the fourth and sixth boosts, respectively, and antisera were assayed for antibody titers to Antigen A.

Antibody titers were determined in sera of immunized mice using an ELISA assay. Ninety six-well microtiter plates (Thermo Scientific) were coated with Antigen A (1 μg/ml) in phosphate-buffered saline (PBS, Irvine Scientific) overnight at 4° C. The following day, plates were washed with phosphate-buffered saline containing 0.05% Tween 20 (PBS-T, Sigma-Aldrich) four times using a plate washer (Molecular Devices). Plates were then blocked with 250 μl of 1% bovine serum albumin (BSA, Sigma-Aldrich) in PBS and incubated for one hour at room temperature. The plates were then washed four times with PBS-T. Sera from immunized mice and pre-immune sera were serially diluted ten-fold in 0.1% BSA PBS-T starting at 1:100 and added to the blocked plates in duplicate and incubated for one hour at room temperature. The last two wells were left blank to be used as secondary antibody control. The plates were again washed four times with PBS-T in a plate washer. A 1:5000 dilution of goat anti-mouse IgG-Fc-Horse Radish Peroxidase (HRP, Jackson Immunoresearch) conjugated secondary antibody was added to the plates and incubated for one hour at room temperature. Plates were again washed eight times with PBS-T and developed using TMB/H₂O₂ as substrate. The substrate was incubated for twenty minutes and the reaction stopped with 1 N H₂SO₄ (VWR). Plates were read on a spectrophotometer (Victor, Perkin Elmer) at 450 nm. Antibody titers were calculated using GRAPHPAD PRISM™ (GraphPad Software, Inc).

Serum titer was calculated as serum dilution within experimental titration range at the signal of antigen binding equivalent to two times above background. Antibody titer for the humoral immune response against a human cell surface receptor (Antigen A) is set forth in FIG. 19.

In a similar experiment, humoral immune responses were determined for mice homozygous for human heavy and κ light chain variable gene loci (H_(κ)) and mice homozygous for a single human V_(H) gene segment, all human D_(H) and J_(H) gene segments operably linked to mouse heavy chain constant regions (1hV_(H) HO) by comparative immunization using influenza viral vaccines FLUVIRIN® (Novartis Vaccines) and FLUMIST® (MedImmune LLC).

Briefly, serum was collected from groups of mice prior to immunization with the above antigen (as described above). Mice (n=5) homozygous for a single human V_(H) gene segment (V_(H)1-69), all human D_(H) and J_(H) gene segments operably linked to mouse heavy chain constant regions (1hV_(H) HO) were immunized intra-nasally (i.n.) with FLUMIST® (live attenuated influenza vaccine) at 1/3 the normal dose/mouse. One normal dose of FLUMIST® contains 10^(6.5-7.5) FFU (fluorescent focus units) of live attenuated influenza vaccine. Therefore, each mouse was primed with 70 μl FLUMIST® on day 1 followed by i.n. boost on days 3, 6, 11, 13, 17, 20 for a total of 6 boosts. No adjuvants were employed in this immunization. The mice were bled on days 15 and 22 after 4th and 6th boosts respectively and antiserum assayed for antibody titers to FLUMIST® (as described above).

In a similar manner, in immunizations with FLUVIRIN®, pre-immune serum was collected from mice prior to initiation of immunization. Mice (n=5) homozygous for a single human V_(H) gene segment (V_(H)1-69), all human D_(H) and J_(H) gene segments operably linked to mouse heavy chain constant regions (1hV_(H) HO) were immunized with FLUVIRIN® (trivalent inactivated influenza vaccine) via footpad (fp.) with 0.75 μg each of hemagglutinin/mouse/boost. Mice were primed on day 1 followed by f.p. boost on days 3, 6, 11, 13, 17, 20 for a total of 6 boosts. No adjuvants were employed in this immunization. The mice were bled on days 15 and 22 after 4th and 6th boosts respectively and antiserum assayed for antibody titers to FLUVIRIN® (as described above).

Serum titer was calculated as serum dilution within experimental titration range at the signal of antigen binding equivalent to two times above background. Antibody titer for the humoral immune response against FLUMIST® and FLUVIRIN® is set forth in FIG. 20.

As shown in this Example, antibody titers generated in 1hV_(H) HO mice were comparable to those generated in mice having a plurality of human V_(H) gene segments (H_(κ)) for both a human cell surface receptor and a viral antigen (e.g., influenza). Thus, mice having immunoglobulin heavy chain loci restricted to a single V_(H) gene segment are capable of mounting a robust immune response to antigen in a manner comparable to mice having immunoglobulin heavy chain loci containing a plurality of human V_(H) gene segments (e.g., 80 V_(H)).

Example 4 Analysis of Antibody Gene Usage and CDR3 Length in Mice Having a Restricted Immunoglobulin Heavy Chain Locus

Splenocytes harvested from mice homozygous for a single human V_(H) gene segment at the endogenous heavy chain locus and homozygous for a replacement of the endogenous κ light chain variable loci with human κ light chain variable loci immunized with a human cell surface receptor (Antigen A) were analyzed for heavy and light chain gene segment usage by reverse-transcriptase polymerase chain reaction (RT-PCR) on mRNA from splenic B cells.

Briefly, spleens were harvested and homogenized in 1×PBS (Gibco) using glass slides. Cells were pelleted in a centrifuge (500×g for 5 minutes), and red blood cells were lysed in ACK Lysis buffer (Gibco) for 3 minutes. Cells were washed with 1×PBS and filtered using a 0.7 μm cell strainer. B-cells were isolated from spleen cells using MACS magnetic positive selection for CD19 (Miltenyi Biotec). Total RNA was isolated from pelleted B-cells using the RNeasy Plus Kit (Qiagen). PolyA⁺ mRNA was isolated from total RNA using the Oligotex® Direct mRNA mini kit (Qiagen).

Double-stranded cDNA was prepared from splenic B cell mRNA by 5′ RACE using the SMARTer™ Pico cDNA Synthesis Kit (Clontech) with substitution of the supplied reverse transcriptase and dNTPs with Superscript® II and dNTPs (Invitrogen). V_(H) and V_(κ) antibody repertoires were amplified from the cDNA using primers specific for IgM, IgG, or Igκ constant regions and the SMARTer™ 5′ RACE primer (Table 6). PCR products were purified using a QlAquick® PCR Purification Kit (Qiagen). A second round of PCR was done using the same 5′ RACE primer and a nested 3′ primer specific for the IgM, IgG, or Igκ constant regions (Table 7). Second round PCR products were purified using a SizeSelect™ E-Gel® system (Invitrogen). A third PCR was performed with primers that added 454 adapters and barcodes. Third round PCR products were purified using Agencourt® AMPure® XP Beads (Beckman Coulter). Purified PCR products were quantified by SYBR® qPCR using a KAPA Library Quantification Kit (KAPA Biosystems). Pooled libraries were subjected to emulsion PCR (emPCR) using a 454 GS Junior Titanium Series Lib-A emPCR Kit (Roche Diagnostics) and bidirectional sequencing using Roche 454 GS Junior instrument according to manufacturer's specifications.

Bioinformatic analysis. The 454 sequences were sorted based on the sample barcode perfect match and trimmed for quality. Sequences were annotated based on alignment of rearranged immunoglobulin sequences to human germline V(D)J segment database using local installation of Igblast (NCBI, v2.2.25+). A sequence was marked as ambiguous and removed from analysis when multiple best hits with identical score were detected. A set of perl scripts was developed to analyze results and store data in mysql database. CDR3 region was defined between conserved C codon and FGXG motif for light and WGXG motif for heavy chains. CDR3 length was determined using only productive antibodies. From the nucleic acid sequences and predicted amino acid sequences of the antibodies, gene usage was identified for IgM-primed (15,650), IgG-primed (18,967), and Igκ-primed (26,804) sequences. Results are shown in Table 8, Table 9, FIG. 21 and FIG. 22.

Table 8 sets forth the percentage of observed human D_(H) and J_(H) gene segments used among IgM-primed (15,650 sequences) and IgG-primed (18,967 sequences) V_(H)1-69 derived heavy chain variable region sequences. Human D_(H)4-4/D_(H)4-11 and human D_(H)5-5/D_(H)5-18 gene segments are presented in Table 8 together due to identical sequence identity between the respective pairs of D_(H) gene segments. Table 9 sets forth the percentage of human V_(κ) and J_(κ) gene segments observed among light chains (26,804 sequences) cognate with V_(H)1-69 derived heavy chain variable regions. Percentages in Tables 8 and 9 represent rounded values and in some cases may not equal 100% when added together.

Amino acid length of the CDR3 region of IgM-primed V_(H)1-69-derived heavy chains is shown in FIG. 21. Amino acid length of the CDR3 region of IgG-primed V_(H)1-69-derived heavy chains is shown in FIG. 22.

As shown in Tables 8 and 9, mice according to the invention generate antigen-specific antibodies containing V_(H)1-69-derived heavy chains, which demonstrate a variety of rearrangements of a human V_(H)1-69 gene segment with a variety of human D_(H) segments and human J_(H) segments. Further, the antigen-specific antibodies contain cognate human light chains containing human V_(κ) domains resulting from a variety of rearrangements of human V_(κ) and J_(κ) gene segments.

TABLE 6 Primer Sequence (5′-3′) 3′ Cg1 outer GGAAGGTGTG CACACCGCTG GAC (SEQ ID NO: 71) 3′ Cg2ac outer GGAAGGTGTG CACACCACTG GAC (SEQ ID NO: 72) 3′ Cg2b outer GGAAGGTGTG CACACTGCTG GAC (SEQ ID NO: 73) 3′ Cg3 outer AGACTGTGCG CACACCGCTG GAC (SEQ ID NO: 74) 3′ mIgM CH1 TCTTATCAGA CAGGGGGCTC TC (SEQ ID outer NO: 75) 3′ mIgκC outer AAGAAGCACA CGACTGAGGC AC (SEQ ID NO: 76)

TABLE 7 Primer Sequence (5′-3′) 3′ mIgG1/2b AGTGGATAGA CWGATGGGGG TG (SEQ ID CH1 inner NO: 77) 3′ mIgG2a/2c AGTGGATAGA CCGATGGGGC TG (SEQ ID CH1 inner NO: 78) 3′ mIgG3 AAGGGATAGA CAGATGGGGC TG (SEQ ID CH1 inner NO: 79) 3′ mIgκM GGAAGACATT TGGGAAGGAC TG (SEQ ID CH1 inner NO: 80) 3′mIgκC-2 GGAAGATGGA TACAGTTGGT GC (SEQ ID inner NO: 81)

TABLE 8 Human D_(H) IgM IgG Human J_(H) IgM IgG 1-1 1.2 6.0 1 7.5 1.5 1-7 39.9 9.0 2 3.3 4.2  1-14 0.5 2.3 3 22.2 12.8  1-20 2.3 1.4 4 51.5 36.4  1-26 3.5 5.7 5 10.5 9.5 2-2 1.1 3.2 6 4.9 29.4 2-8 0.7 0.6  2-15 0.3 1.2  2-21 0.7 0.3 3-3 6.3 5.2 3-9 0.6 0.6  3-10 0.9 10.3  3-16 0.9 2.0  3-22 5.1 2.7  4-4/4-11 1.5 4.0  4-17 1.5 4.7  4-23 11.5 2.4  5-12 1.1 1.8  5-5/5-18 1.3 3.2  5-24 0.3 3.3 6-6 1.8 4.5  6-13 6.1 7.4  6-19 3.0 5.1  6-25 0.1 0.6  7-27 3.3 7.3

TABLE 9 Human Vκ % Observed Human Jκ % Observed 1-5 3.4 1 28.1 1-6 1.3 2 25.3 1-8 0 3 12.1 1-9 1.3 4 22.5  1-12 1.0 5 11.1  1-13 0  1-16 2.5  1-17 3.6  1-22 0  1-27 0.5  1-32 0  1-33 14.3  1-35 0  1-37 0  1-39 1.6 2-4 0  2-10 0  2-14 0  2-18 0  2-19 0  2-23 0  2-24 0.7  2-26 0  2-28 0  2-29 0  2-30 1.9  2-36 0  2-38 0  2-40 1.5 3-7 0  3-11 2.7  3-15 3.9  3-20 41.2  3-25 0  3-31 0  3-34 0 4-1 13.2 5-2 0.1  6-21 0 7-3 0 

1. A rat or mouse having a restricted immunoglobulin heavy chain locus characterized by the presence of a single human V_(H) gene segment, one or more human D_(H) gene segments, and one or more human J_(H) gene segments.
 2. The rat or mouse of claim 1, wherein the mouse comprises a deletion of all or substantially all endogenous V_(H), D_(H), and J_(H) gene segments.
 3. The mouse of claim 1, wherein the single human V_(H) gene segment is selected from V_(H)1-2, V_(H)1-69, V_(H)2-26, V_(H)2-70, V_(H)3-23. 4.-5. (canceled)
 6. The rat or mouse of claim 1, wherein the single human V_(H) gene segment is operably linked to a human or non-human immunoglobulin constant region gene.
 7. The rat or mouse of claim 6, wherein the single human V_(H) gene segment is operably linked to a mouse, rat, or human constant region gene.
 8. The rat or mouse of claim 1, further comprising a one or more human immunoglobulin V_(L) gene segments operably linked to one or more human J_(L) gene segments.
 9. The rat or mouse of claim 8, wherein the one or more human V_(L) gene segments and/or the one or more human J_(L) gene segments are selected from human κ and human λ gene segments.
 10. The rat or mouse of claim 8, wherein the one or more human immunoglobulin V_(L) gene segments and the one or more human J_(L) gene segments are operably linked to a non-human light chain constant gene.
 11. The rat or mouse of claim 10, wherein the non-human light chain constant gene is selected from a mouse κ or λ constant region gene.
 12. A mouse comprising, in its germline, a replacement at an endogenous immunoglobulin heavy chain locus of all or substantially all endogenous V_(H), D_(H), and J_(H) gene segments with single human V_(H) gene segment and/or polymorphic variants thereof, one or more human D_(H) gene segments and one or more human J_(H) gene segments.
 13. The mouse of claim 12, further comprising a replacement at an endogenous immunoglobulin light chain locus of all or substantially all endogenous V_(L) and J_(L) gene segments with one or more human V_(L) and one or more human J_(L) gene segments.
 14. (canceled)
 15. A cell or tissue derived from the rat or mouse of claim
 1. 16. A method of making a nucleic acid sequence encoding a human V_(H) domain, comprising (a) immunizing a rat or mouse of claim 1 with an antigen of interest; (b) allowing said mouse to mount an immune response to the antigen of interest; and, (c) obtaining a nucleic acid sequence encoding a human V_(H) domain from said mouse. 17.-19. (canceled)
 20. The method of claim 16, wherein the immunoglobulin V_(H) region sequence is at least 95% identical to SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66 or SEQ ID NO:
 68. 21. The method of claim 16, wherein the immunoglobulin V_(H) region sequence comprises SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO:
 68. or a polymorphic variant thereof.
 22. The method of claim 16, wherein the immunoglobulin V_(H) region sequence encodes a protein that is at least 95% identical with SEQ ID NO: 61, SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67 or SEQ ID NO:
 69. 23. The method of claim 16, wherein the method further comprises making a nucleic acid sequence encoding a human V_(L) domain that is cognate with the human V_(H) domain, comprising isolating a B cell encoding the human V_(H) domain and the human V_(L) domain from said mouse and obtaining therefrom the sequence of the heavy and light chain variable domains.
 24. The method of claim 23, wherein the human V_(L) domain is a V_(κ) domain.
 25. The method of claim 16, wherein the mouse comprises a deletion of the endogenous immunoglobulin heavy chain locus and the endogenous κ light chain.
 26. A rat or mouse comprising an endogenous immunoglobulin heavy chain locus, wherein the endogenous immunoglobulin heavy chain locus consists essentially of a) one or more polymorphic variants of a single human V_(H) gene segment, b) one or more human D_(H) gene segments, and c) one or more human J_(H) gene segments, wherein the single human V_(H) gene segment is a polymorphic V_(H) gene segment associated with a high copy number in human populations, and wherein the single human V_(H) gene segment, one or more human D_(H) gene segments, and one or more J_(H) gene segments are operably linked to a non-human immunoglobulin heavy chain constant region gene.
 27. A cell or tissue derived from the rat or mouse of claim
 26. 28. A method of making a nucleic acid sequence encoding a human V_(H) domain, comprising (a) immunizing a rat or mouse of claim 26 with an antigen of interest; (b) allowing said mouse to mount an immune response to the antigen of interest; and, (c) obtaining a nucleic acid sequence encoding a human V_(H) domain from said mouse. 